Blood products, for which a platelet count was not performed, were distributed.
Blood products, prepared without additive (Optisol), were distributed.
Nebraska; Ohio; Pennsylvania; New Jersey; Switzerland
Blood products, which were collected from a donor who traveled to a malarial endemic area, were distributed.
Blood product, incorrectly labeled as negative for the Jka red cell antigen, was distributed.
Blood products, collected using an expired blood collection set were expired, were distributed.
Blood and Blood Products for Reprocessing
Blood products, which were not prepared in accordance with specifications, were distributed.
Blood product, which was collected from a donor who traveled to a malarial endemic area, was distributed.
Blood product, in which an extended collection time for FFP, was distributed.
Platelets Pheresis Leukocytes Reduced Irradiated
Blood product, which did not meet the acceptable product specifications, was distributed.
Blood products, collected from a donor with a history of Hepatitis, were distributed.
Red Blood Cells Leukocytes Reduced Irradiated
Red Blood Cells (Apheresis) Leukocytes Reduced
Blood products, in which quality control and distribution of products did not meet specifications, were distributed.
Blood product, which was collected from a donor in which donor suitability was not adequately determined, was distributed.
Blood products, collected from a donor who traveled to an area considered endemic for malaria, were distributed.
Blood products, collected from a donor who was previously HIV-1/2 reactive, were distributed.
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Blood products, collected from donors, whose suitability to donate was not adequately determined, were distributed.
Blood products, in which viral testing/testing performed, interpreted, or documented incorrectly, were distributed.
Blood product, in which donor donated without an acceptable arm check, was distributed.
Blood products, collected from a donor with a history of hepatitis and fatty liver disease, were distributed.
Blood products, collected from a donor whose scheduled physical examination was incomplete, were distributed.
Blood products, which were collected from a donor who traveled to malarial endemic areas, were distributed.
Blood products, collected from a donor whose physical was overdue, were distributed.
Blood products, collected from donors who did not have a complete physical examination, were distributed.
Platelets Pheresis Leukocytes Reduced, Apheresis
Blood products, collected from a donor who traveled to a malarial endemic area, were distributed.
Round Fresh Tomatoes sold in bulk boxes, 20 lbs
The product has the potential to be contaminated with E. coli 0157: H7.
US Distribution including the states of CA, CO, FL, KS and PA.
Laserworld RGB & Piko Nano RGB Models   All models are laser light show projectors, and will be used as such.
All projectors distributed between 2008 and 2012, including, but not limited to, the Proline Series AG, Revolution Series AG, Club Series AG, Clus Series, Pure Light Series, and Revolution Series AG
Total distribution of more than 500 units between July1, 2008, and June 30, 2012
A potential lack of certification, and/or missing laser certification, laser safety warning and administrative labels, and potentially incomplete Performance Feature set and incomplete User Information were discovered.
MO; GA; IL; TN; TX; KY; AR; CA; France; Saipan; Guam
Nationwide distribution: USA including states of: AR, CA, FL, IL, LA, NC, NJ, NY, MD, ME, MN, SC, TN, TX, VA, WI, and WV.
Outlook ES pump is intended for use with B. Braun Medical Inc. Horizon Pump IV Sets. Used to regulate the flow of primary and secondary fluids when positive pressure is required. The infusion system is capable of delivering fluid from a negative head height (when the IV fluid container is lower than the pump), and provides clinically accepted volumetric accuracy for all standard IV fluids, including blood, lipid, and Total Parenteral Nutrition (TPN). Model number: 621-300ES and 621-400ES. To deliver a broad range of drugs with use with the B. Braun Medical Inc. Horizon Pump IV Sets.
Model number: 621-300ES and 621-400ES.  Multiple serial numbers affected.
This notice is being provided in follow up to the field correction initiated by B. Braun Medical Inc. on August 26, 2011 due to an issue in which the Outlook ES Safety Infusion System may halt infusion but the ''RUN'' Light Emitting Diodes (LEDs) on the front display continue to advance as if the pump were infusing. The pump emits a backup alarm, but there are no visual indicators that the infusion has stopped.  The issue can potentially be observed in some  Outlook ES pump models 300ES and 400ES with Compact Flash card. It is possible that under infusion could occur because the user may see a visual indication that the pump is running when it is not. B. Braun Medical Inc. has identified that not all of the affected Outlook ES pumps were listed in the original notification of this field correction.  Although these pumps were not identified in the previous notice, these pumps were upgraded, if available, during field services.
Rochester Eye and Human Parts Bank, Inc.
Human Cornea, not tested to adequately and appropriately reduce the risk of transmission of relevant communicable disease agents or diseases, was distributed.
Synthes Cannulated Distal Femoral Nail (Trauma Nail), Part Number 450.851S, 420MM-Sterile.  Orthppedic implant device.
Part Number 450.851S, Lot Number 7065061
Firm discovered that a nail that was within the scope of a previous Trauma Nail recall had been distributed.
SPIRIVA HandiHaler (Tiotropium Bromide Inhalation Powder) Capsules 18 mcg per dose, Rx only, a) 10 count blister (NDC 0597-0075-27), b) 30 count blister (NDC 0597-0075-41), c) 90 count blister (NDC 0597-0075-47), d) 5 count blister physician sample (NDC 0597-0075-75), Manufactured by: Boehringer Ingelheim (BI) Pharma, GmbH & Co. KG, Ingelheim, Germany
Presence of Foreign Substance: This recall is being conducted due to the potential for extrinsic foreign particles in the API used to manufacture SPIRIVA Handihaler
Blood products, collected from an ineligible donor, were distributed
Interstate Blood Bank, Inc. of Wisconsin
Blood products, collected from an ineligible donor, were distributed.
Wellmont Health System Dba Marsh Regional Blood Center
Blood products, collected from a donor who reported testing positive for hepatitis, were distributed
Platelets Pooled Leukocytes Reduced Irradiated
Blood product, which did not meet the acceptable product specification for release, was distributed.
Blood products, which were collected from a donor who traveled to a malarial endemic area, were distributed
Blood products, collected from a donor who was at risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed
Midsouth Eye Bank for Sight Restoration Inc
Human corneas, recovered from a donor whose donor eligibility determination failed to ensure that the donor was free from risk factors for, and clinical evidence of infection due to relevant communicable disease agents and diseases, were distributed.
Tennessee; Ohio; Colorado; Indiana; New York; Texas
Human tissue allografts, recovered from a donor whose donor eligibility determination failed to ensure that the donor was free from risk factors for, and clinical evidence of infection due to relevant communicable disease agents and diseases, were distributed.
Tennessee; Oklahoma; Korea, Republic Of(South); Alabama; Louisiana; Florida; Indiana; Texas
Worldwide distribution - US: (nationwide) including the states of  AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IL, IN, KS, KY, LA, MA, MI, MN, MO, NC, NE, NV, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA, WI and  WV., and the countries of : Australia, Canada, Columbia, Lebanon, Mexico and Saudi Arabia.
Responder 5 is a nurse call communication system that connects patients with staff in a hospital.  The nurse call system also connects team members and departments from radiology, physical therapy, transport, environmental services and more.       Responder 5 is used in hospitals and long term patient care facilities to allow for remote communications between patients and patient monitoring devices and healthcare providers
1) Product Code 351000 (Branch Regional Controller);  2) Product Code 352000 (Corridor Light);   3) Product Code 352020 (Domeless Controller)
Product Code 351000: 385 units; Product Codes 352000 and 352020: 14,808 units (total)
A counterfeited electronic component was identified in the products affected. The component, a data transceiver (transmitter/receiver), is associated with the intercommunication of these devices in the Responder 5 system across the L-Net data path.  Failure of a data transceiver results in the loss of nurse call functionality in the associated room, and may disrupt communications on the L-Net run, affecting nurse call communications across multiple rooms.
Worldwide Distribution-USA (nationwide) including DC and the states of AL, AR, AZ, CA, CO, DE, FL, GA, IN, KY, MA, MD, MI, MN, MS, NC, NM, NV, NY, OH, OK, PA, SC, TN, TX, VT, WI & WV, and the countries of Australia, Austria, Bosnia & Herzegovina, Chile, China, Croatia, Denmark, Equatorial Guinea, France, Germany, Greenland, Iceland, Indonesia, Israel, Japan, Kazakhstan, Netherlands, Nigeria, Norway, Poland, Romania, South Africa, South Korea, Sweden, Switzerland, Taiwan, United Arab Emirates, United Kingdom & Vietnam.
Brilliance CT   6, M/N 728256; Brilliance CT 16 M/N 728246; Brilliance CT 40, M/N 728235 & Brilliance CT 64 M/N  728231, Philips Healthcare, Cleveland, OH 44143.   Intended to produce cross-sectional images of the body by computer reconstruction.
The patient support may move in an unintended manner if the footswitch cover impinges on the footswitch.
Two restaurants -  one in Alaska and one in Oregon
Batch number 71013 (this represents the production date)   Best by date is 12/10/13
Frozen Hot Smoked Vacuum-Packed Salmon packaged in 1.5 lb packages is being recalled due to missing information on the label.  Specifically, ''Important:  Keep Frozen Until Used.  Thaw under Refrigerated immediately before use''.  Failure to provide instructions on the label for proper storage and handling of the product can cause Clostridium botulinum to grow and produce toxin.
Worldwide Distribution - USA including AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI,  and WV.  Internationally to Canada, Argentina, Australia, Austria, Belarus, Belgium, Brazil, Brunei, Chile, China, Colombia, Costa Rica, Czech Republic, Denmark, Dubai, Finland, France, Germany, Great Britian, Greece, Guatemala, Hong Kong, Hungary, India, Ireland, Israel, Italy, Japan, Korea, Kuwait, Luthuania, Luxembourg, Malaysia, Mexico, Netherlands, New Zealand, Norway, Panama, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Uruguay, Venezuela, and Viet Nam.
ACL TOP (Base); PN 0000280000   Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or fibrinolysis testing in the assessment of thrombosis and/or hemostasis. The systems provide results for both direct hemostasis measurements and calculated parameters.
Nov 2003 - Nov 2011, Serial Numbers 02110101 through 11111174
Potential carryover issue that can can cause shortened APTT clotting times on the instrument.
ACL TOP 700; PN 0000280010   Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or fibrinolysis testing in the assessment of thrombosis and/or hemostasis. The systems provide results for both direct hemostasis measurements and calculated parameters.
Start SN and Date:  09080100, Aug 2009 End SN and Date: 13070559, July 2013
ACL TOP CTS; PN 0000280020   Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or fibrinolysis testing in the assessment of thrombosis and/or hemostasis. The systems provide results for both direct hemostasis measurements and calculated parameters.
Start SN and Date:  06020101, Feb 2006; End SN and Date: 10080662, Aug 2010
ACL TOP 700 LAS; PN 0000280030   Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or fibrinolysis testing in the assessment of thrombosis and/or hemostasis. The systems provide results for both direct hemostasis measurements and calculated parameters.
Start SN and Date:  08120100, Dec 2008; End SN and Date: 13070172, July 2013
ACL TOP 700 CTS; PN 0000280050   Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or fibrinolysis testing in the assessment of thrombosis and/or hemostasis. The systems provide results for both direct hemostasis measurements and calculated parameters.
Start SN and Date:  09120101, Dec 2009; End SN and Date: 13070304, July 2013
ACL TOP 300 and ACL TOP 300 CTS (Japan); PN 0000280060   Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or fibrinolysis testing in the assessment of thrombosis and/or hemostasis. The systems provide results for both direct hemostasis measurements and calculated parameters.
Start SN and Date:  12060256, Jun 2012; End SN and Date: 13070837, July 2013 and Start SN and Date: 11120131J, Dec 2011; End SN and Date: 13060320J, Jun2013
ACL TOP 500 CTS; PN 0000280040   Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or fibrinolysis testing in the assessment of thrombosis and/or hemostasis. The systems provide results for both direct hemostasis measurements and calculated parameters.
The recalled products were distributed to MD, CT, PA, and NY
Liquid Yeast Cream, Bulk, in tanker truck quantities, refrigerated 33F-45F
Bulk liquid yeast is contaminated with Salmonella.
Nationwide Distribution including AR, AZ, CA, CO, FL, IL, KY, LA, MI, NJ, NY, OH,OK, OR, SC, TX, UT, and WA.
DiaScreen Liquid Urine Controls: Positive and Negative Assayed Liquid Quality Controls for use with Dipsticks in Routine Urinalysis; Product Number D76004 (4x12 mL bottles) consists of: 2x12mL Positive controls [and] 2x12mL Negative controls; Manufactured for ARKRAY USA, Inc.; Minneapolis, MN 55439   Diascreen liquid urine control is a synthetic control designed to react with commercial urine dipsticks to register listed responses on color reagent pads. It is intended for use in a clinical laboratory as a urine control for qualitative procedures used in chemical determinations. The control is intended to be used exactly as if it were a patient sample to assist in the assessment of the listed analytical procedures.
Product Number: D76004;  Lots: All Lots;   Independence Medical Catalog Number: CJD76004
The products may have been stored at temperatures outside their required storage conditions.
Hemoccult II BRAND SENSA elite; MATERIALS AND REAGENTS; Hemoccult II SENSA elite Slides (Test Cares) containing guaiac paper; Hemoccult SENSA Developer-a developing solution containing a stabilized mixture of less than 4.2% hydrogen peroxide, 80% denatured ethyl alcohol and enhancer in an aqueous solution; Applicator Sticks; Patient Screening Kit Dispensing Envelopes with Patient Instructions; Flushable Collection Tissues; Mailing Pouches (for returning completed Test Cares); Hemoccult II SENSA elite Product Instructions; Beckman Coulter, Inc.; 250 S. Kraemer Blvd.; Brea, CA 92821   The Hemoccult II SENSA elite test is a rapid, convenient and qualitative method for detecting fecal occult blood which may be indicative of gastrointestinal disease. It is not a test for colorectal cancer or any other specific diseases. The Hemoccult II SENSA elite test is recommended for professional use as a diagnostic aid during routine physical examinations, for hospital patients to monitor for gastrointestinal bleeding in patients with iron deficiency anemia or recuperating from surgery, peptic ulcer, ulcerative colitis and other conditions, and in screening programs for colorectal cancer when the Patient Instructions are closely followed. Serial fecal specimen analysis is recommended when screening symptomatic patients. The Hemoccult II SENSA elite test and other unmodified guaiac tests are not recommended for use with gastric specimens.
Product Number: 9964130;  Lots: All Lots;   Independence Medical Catalog Number: 9964130
ProTime Microcoagulation System; PROTIME CUVETTE AND PROTIME3 CUVETTE; Store the foil-pouched cuvettes refrigerated 2-8C (36 - 36F); MATERIALS PROVIDED; ProTime cuvettes with Tenderlett Plus; or; Protime3 cuvettes with Tenderlett Plus LV; Product Instructions; Antiseptic, gauze (with self-test package only); International Technidyne Corporation; 8 Olsen Avenue; Edison, NJ 08820 USA; a subsidiary of Thoratec Corporation   The ProTime Microcoagulation System consists of a portable, battery operated instrument and disposable cuvette for quantitative determination of prothrombin time (PT) from fingerstick whole blood or anticoagulant-free venous whole blood. There are two different types of cuvettes available for use with the ProTime Microcoagulation System: a ProTime cuvette and a ProTime3 cuvette. The ProTime cuvette is black color coded and utilizes three channels for the PT assays and two channels for integral controls. It requires approximately 65 ul of blood (approximately 3 drops). The ProTime3 cuvette is blue color coded and utilizes one channel for PT assay and two channels for integral controls. The ProTime3 cuvette requires approximately 27 ul of blood (approximately 1 large drop). The ProTime Microcoagulation System is intended for professional use in the management of patients treated with oral anticoagulants or for patient self-testing.
*** 1) Product Number: PRO3-25;  Lots: All Lots;   Independence Medical Catalog Number: 55L2101002;   *** 2) Product Number: PRO5-25;   Lots: All Lots;   Independence Medical Catalog Number: ICPRO525
Undeclared allergens: wheat. The list of ingredients declare ''semolina durum'' but not the common name ''wheat''.
Undeclared allergens: wheat. and soy One of the ingredients is ''Super Pan'' that contains wheat as a sub-ingredient. The coconut milk is another ingredient that contains ''soy lecithin'' and it is undeclared.
VisuALIF,System consisting of a 'U' shaped PEEK block in two footprint configurations, four heights and three lordosis angles., part number:  0301-1410.   Intended to be implanted via an open anterior approach.
The product has the potential to be laser marked as a Medium when it actually is a Small.
distributed in Idaho, Oregon and Washington.
Frozen dough balls are sold under brand name Winco or Tasty Bake:   Item # 04018 is 17 oz wheat dough ball, Winco brand, individually wrapped in plastic bag with label for retail use, UPC 0 31693 04018 9;    Item # 00518 is 17 oz white dough ball, Winco brand, individually wrapped in plastic bag with label for retail use, UPC 0 31693 00518 8;    Item # 00520 is Tasty Bake original 20 oz dough ball, BULK packed with 30 individual plastic bags per case for food service use,UPC 0 31693 00520 1;     Item # 00525 is Tasty Bake original 25 oz dough ball, BULK packed with 24 individual plastic bags per case for food service use, UPC 0 31693 00525 6;    Item # 00530 is Tasty Bake original 30 oz dough ball, BULK packed with 20 individual plastic bags per case for food service use,UPC 0 31693 00530 0.    The Winco's label is read in parts: ''***Pizza Dough***Roll out crust to desired size***Top with favorite toppings***Baked at 400F  for 15 to 20 minutes or until golden brown***''.    The Cooking instructions is labeled in parts: ''***CRUST & DOUGH HANDLING***DOUGH BALLS***Cooking Guidelines for Dough Balls***Deck***Oven Temp 450-475F***Cook time 12-18 minutes****Conveyor***Oven Temp 500F***Cook time 5-9 minutes***Convection***Oven Temp 400-425F***Cook time 7-12 minutes***Tasty Bake, Inc.***1945 8th Street***Baker City, OR 97814***(800) 753-2112***(541) 523-5323***Fax: (541) 523-4764***
Julian Dates 213-220    It interprets that product was made on August 1 through August 8.
Frozen dough ball was processed with Baker City (Oregon) water and it has a potential to be contaminated with Cryptosporidium. The Boil Water Notice was issued on 7/31/13 by Baker County and Baker City officials in Oregon
USA Nationwide Distribution in the state of GA, AK, WA, and CA.
T8 REMOVAL HEAD, REF 8910641, QTY: 1 EA,    Product Usage:  The non-sterile T8 Removal Diriver is used with the Spire and Spire Z Spinal System in conjunction with the set screwdriver to remove the implant during removal surgery. The set screw driver is attached to the end of the removal head and used to disengage the remaining portion of the set screw within the device.
One lot of the T8 Removal Head had incorrect hardness specification, which could result in the T8 Removal head failing during removal of the CD Horizon Spire and Spire Z Spinal System implant.  There is a potential for tissue damage to occur and/or minor surgical delay to remove the remaining fragments of the tip.
Benefiber, Fiber plus Calcium Supplement, Wild Berry Chewables 90ct, sugar free, chewable tablets bottle. Novartis Consumer Health, Inc, Parsippany, NJ.
The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
Benefiber, Fiber Supplement, Orange Creme Chewables, Sugar Free, 36ct and 100ct chewable tablet bottles. Novartis Consumer Health, Inc, Parsippany, NJ.
Benefiber, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, Parsippany, NJ.
Benefiber, Fiber Supplement, Assorted Fruit, Sugar Free, 100ct chewable tablets. Novartis Consumer Health, Inc, Parsippany, NJ.
Benefibre, Orange Creme Chewables, 36ct and 100ct chewable tablet bottles.  Foreign labeling: Novartis Consumer Health Canada Inc, Mississauga, ON.
US Nationwide Distribution including the states of AZ, MI, IN, UT, CT, AL, NY, PA, IL, MD, CA, MA, IA, OH, MS and MO.
Juno DRF System. Mobile X-ray system   These are general, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
It has been discovered that the Air Kerma rate information is inconsistent in Continuous Fluoro modes 30x30 (12''x12'') and 15x15 (6''x6). This could result in a deviation of the displayed values of Air Kerma Rate and Cumulated Air Kerma from the actual values greater then +/-35% and then in a failure to comply with the requirements of 21 CFR 1020.32(k)(6
Worldwide Distribution - USA Nationwide in the following states: AK, AZ, CA, FL, GA, IL, KY, LA, MA, MD, MN, NE, NJ, NM, NY, OH, OR, PA, TX, VA and WA; and countries of Canada and Mexico.
Sonogage EyeScan, A-Scan Biometer,    Product Usage:  A-Scan Biometer diagnostic device for measurement of axial eye length.
During an FDA inspection on 7/15-26/2013, it was discovered that the firm lacked registration and 510(k) clearance for the device.
Worldwide Distribution - USA (nationwide)  Canada, Europe: Austria, Belgium, Cyprus, Czech Republic, Denmark, Germany, Greece, Finland, France, Italy, Ireland, Luxembourg, Netherlands, Norway, Poland, Portugal, Russia, Slovenia, Spain, Sweden, Switzerland, Turkey, Ukraine and United Kingdom, Asia-pacific: Australia, China, Dubai, Hong Kong, India, Japan, Malaysia, New Zealand, Philippines, Sri Lanka, Singapore, South Korea, Taiwan, Thailand, Argentina, Bermuda, Brazil, Chile, Colombia, Costa Rica, Israel, Mexico, Puerto Rico, South Africa, and Venezuela.
BIORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture; Part Number: 72200775   Biodegradable suture anchor
Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
BIORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture; Part Number: 72200774   Biodegradable suture anchor
BIORAPTOR 2.9 mm Suture Anchor with DURABRAID'' Suture; Part Number: 72200783   Biodegradable suture anchor
BIORAPTOR 2.9 mm Suture Anchor Straight, pack of 2 ULTRABRAID Suture; Part Number: 72200690   Biodegradable suture anchor
BIORAPTOR 2.9 mm Suture Anchor, pack of 1 ULTRABRAID Suture: 72200689   Biodegradable suture anchor
OSTEORAPTOR 2.3 mm  Suture Anchor with ULTRABRAID COBRAID Suture, Blue; Part Number:  72201993   Biodegradable suture anchor
OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture, White / Blue ; Part Number:  72201995   Biodegradable suture anchor
OSTEORAPTOR 2.3 mm with 1 ULTRABRAID Suture, White; Part Number:  72201991   Biodegradable suture anchor
OSTEORAPTOR 2.3 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Black; Part Number:  72201992   Biodegradable suture anchor
OSTOSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Blue; Part Number:  72201994   Biodegradable suture anchor
OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture, White / Black; Part Number:  72201996   Biodegradable suture anchor
OSTEORAPTOR 2.9  mm Suture Anchor with 1 ULTRABRAID Suture, White; Part Number:  72202165   Biodegradable suture anchor
OSTEORAPTOR CURVED 2.3 mm Suture Anchor ULTRABRAID COBRAID Suture, Black; Part Number:  72203291   Biodegradable suture anchor
OSTEORAPTOR CURVED 2.3 mm Suture Anchor SA ULTRABRAID COBRAID Suture, Blue; Part Number:  72203290   Biodegradable suture anchor
TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture, White / Blue; Part Number:  72202597   Biodegradable suture anchor
TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture, Blue / Black; Part Number:  72202624   Biodegradable suture anchor
TWINFIX Ultra HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture, Blue / Black; Part Number:  72202626   Biodegradable suture anchor
TWINFIX Ultra HA 6.5 mm with 2 ULTRABRAID Suture, Blue / Black; Part Number:  72202631   Biodegradable suture anchor
TWINFIX Ultra PLLA/HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture, White / Black: Part Number: 72202602   Biodegradable suture anchor
TWINFIX ULTRA PLLA/HA 5.5 mm Suture Anchor with 3 ULTRABRAID Suture: Part Number: 72202603   Biodegradable suture anchor
TWINFIX'' Ultra PLLA/HA 6.5 mm with 2 ULTRABRAID'' Suture, White / Black: Part Number: 72202608   Biodegradable suture anchor
TWINFIX Ultra PLLA/HA 6.5 mm with 3 ULTRABRAID Suture; Part Number: 72202610   Biodegradable suture anchor
RAPTORMITE'' 3.7 mm PLLA with two ULTRABRAID'' Sutures Size 0 and Needles; Part Number: 72201805   Biodegradable suture anchor
TWINFIX'' Ultra 4.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-COBRAID'') with Needles; Part Number: 72202612   Biodegradable suture anchor
TWINFIX Ultra 5.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-COBRAID) with Needles; Part Number: 72202616   Biodegradable suture anchor
TWINFIX Ultra 6.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-COBRAID) with Needles; Part Number: 72202620   Biodegradable suture anchor
Worldwide Distribution - USA including AL, AZ, AR, CA, CO,CT, FL, GA, HI, IL, IN,KS,KY, LA, MD, MA, MI, MN, MO, NE, NV, NJ, NY, NC, OH, OR,PA, TN, TX, UT,VA, WA, and WI.  Internationally to GERMANY, CANADA, BELGIUM, NETHERLANDS, HONG KONG, NEW ZEALAND, AUSTRALIA, INDIA, KOREA, SINGAPORE AND UNITED ARAB EMIRATES, JAPAN, JAMAICA..
3M Scotchcast, Wet or Dry Cast Padding, Catalog Numbers WDP2, WDP3, WDP4, and WDP6.     Intended for use in constructing casts for either wet or dry immobilization.
1207 cases (4 puches per case, 20 rolls per pouch)
3M is conducting a voluntary product recall of selected lots of 3M'' Scotchcast'' Wet or Dry Cast Padding.   Upon investigation of a health care provider feedback, and confirmed with internal testing, it was found that the cast padding material does not consistently repel water.  Lack of repellency may result in prolonged cast dry times after exposure to wet conditions.      There have been no reports of patient injury associated with this material to date.
.Worldwide Distribution - USA including Puerto Rico and  the states of AL, AZ, CA, CO,CT, FL, GA, IL, KY, MD, MA, MI, MN, NE, NJ, NC, OH, OR, PA and TX., and the countries of  CANADA, MEXICO, HONG KONG, SOUTH AFRICA, ARGENTINA, COLOMBIA, ISRAEL, AUSTRALIA, BELGIUM, FINLAND,FRANCE, GERMANY, ITALY, NETHERLANDS, SLOVENIA,  SPAIN, SWITZERLAND and UNITED KINGDOM
AEQUALIS Reversed II or AEQUALIS Fracture Impactor.  These products are contained within the  Aequalis reversed II Instrument set tray no.YKAD83 and the  Aequalis reversed fracture instrument set tray no.YKAD95. The items affected are  MWD21, MWD023, MWD024 and MWD025.   The impactor is an instrument used during shoulder arthroplasty; it is not implanted. The impactor is used to set the glenoid sphere, poly insert, spacer, and hemi adapter into place during surgery. The impactor is a two piece instrument which consists of a tip and a handle. The tip is made of plastic and metal that is pressed together for assembly.
Following the identification of the disassociation of an impactor tip during surgery, Tornier is initiating a voluntary recall of all lots of Aequalis Reversed II and Reversed Fracture impactors.  Upon review of the event, Tornier determined that a redesign of the instrument was warranted.  These products are contained within the Aequalis Revered II instrument set tray no YKAD83 and the Aequalis Revered Fracture instrument set tray no YKAD95.
Nationwide Distribution (US), including the states of NY, MN, NJ, PA, FL, MD, and VA.
Vygon 14 Microbore Extension Set with Bionector, CMS-814-1. The CMS-814-1 is a 14 inch extension set used to administer IV fluids.
Microbore tubing disconnecting from male luers on the extension sets.
Central Dressing Change Kit;  AMS-8464CP- 6.  Vygon Central Dressing Change Kit contains: 1 Pair Nitrile Gloves W/Wallet, Powderfree 1 Face Mask 1 Polylined Drape, 13'' X 18'' 1 ChloraPrep***, 3ml Applicator W/Insert 1 Pkg. Alcohol Swabsticks (3/Pkg.) 1 14'' Extension Set W/Bionector*** 2 Dressing Sponges, 2'' X 2'' 1 Foam Strip, 8/5cm X 1cm 1 3M*** Tegaderm *** IV Dressing W/CHG, 2 1/2'' X 4 1/2'' *** Vygon MFG Dover, NH 03820***''
Undeclared allergens: Yellow #5 and Yellow #6
Professor Zim Zam's Extraordinary Sweets; Dark Chocolate with Sea Salt;  All Natural, 55% Cocoa;  Net Wt. 0.35 oz (9.9g)    Go Picnic:  Distributed by Go Picnic Brands, Chicago, IL 60613;  Made in USA
Two consumer complaints of allergic reactions for Zim Zam products packed in a picnic type lunch that declares it is vegan.  G. Debbas Chocolatier does not claim that their product facility is vegan, as they do make product that contain milk.
Professor Zim Zam's Extraordinary Sweets; Dark Chocolate with Rice Crisps;  All Natural, 55% Cocoa;  Net Wt. 0.35 oz (9.9g)    Go Picnic:  Distributed by Go Picnic Brands, Chicago, IL 60613;  Made in USA
Professor Zim Zam's Extraordinary Sweets; Dark Chocolate with Orange;  All Natural, 55% Cocoa;  Net Wt. 0.35 oz (9.9g)    Go Picnic:  Distributed by Go Picnic Brands, Chicago, IL 60613;  Made in USA
Nationwide Distribution (US), including the states of IN, MD, MS, NC, OH, PA, SC, and TX.
Cypher MIS Screw System, Biomet Spine Parsippany, NJ 07054. The Cypher MIS Screw System is a non-cervical spinal fixation device. 1)Screw Tower - REF 14-501660  2) Rod Reduce - REF 14-501661  3) Counter Torque - REF 14-501662
Several complaints were reported to exhibit screw head splay in the Cypher MIS Screw System.
Acetylcysteine 20% Solution, Preservative Free, 4 mL Sterile Single Dose Vial, Not for Injection, Sterile Solution For Office Use Only, JCB Laboratories, Wichita, KS.
Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.
Sodium Thiosulfate 25%, 250 mg/mL (12.5 g/50mL), PF Sterile Solution for Injection, 50 mL Single Dose Vial, For Office Use Only, JCB Laboratories, Wichita, KS.
Sodium Citrate 4% containing Gentamicin 320 mcg/mL, Solution for Injection, 30 mL Multi Dose Vial, Sterile Solution For Office Use Only, JCB Laboratories, Wichita, KS.
Sodium Citrate 4% Solution for Injection, 30 mL Multi Dose Vial, Sterile Solution for Office Use Only, JCB Laboratories, Wichita, KS.
Epinephrine 1:1,000 (1mg/mL) Sterile Solution for injection, Preservative Free/Sulfite Free, 1-mL Single-Use Syringe, Sterile Solution For Office Use Only, JCB Laboratories, Wichita, KS.
Dextrose 50% Preservative Free SDV Injection Solution, 50 mL Single dose vial, IV Administration, Compounded by Leiter's Compounding Pharmacy, 1700 Park Ave., # 30, San Jose, CA 95126
Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial contamination found after investigation at contract testing laboratory discovered that OOS results were reported to customers as passing.  Hence the sterility of these products cannot be assured.
Hyaluron (hyaluronidase) 150 units/mL Preserved Solution, 1 mL, Multi Dose Vial, Compounded by Leiter's Compounding Pharmacy, 1700 Park Ave., # 30, San Jose, CA 95126
Bevacizumab (Avastin) 2.5mg/0.1mL  PF Inj., 0.1 mL syringe, Compounded by Leiter's Compounding Pharmacy, 1700 Park Ave., # 30, San Jose, CA 95126
Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial contamination found after investigation at contract testing laboratory discovered that OOS/failed results were reported to customers as passing.  Hence the sterility of the products cannot be assured.
Lidocaine/Phenylephrine PF 1%/1.5% Injectible vials, 1 mL Single Use Vial, Compounded by Leiter's Compounding Pharmacy, 1700 Park Ave., # 30, San Jose, CA 95126
Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial contamination found after investigation at contract testing laboratory discovered that OOS/failed results were reported to customers as passing.  Hence the sterility of these products cannot be assured.
Worldwide Distribution-USA including the states of IL, MN, NJ, NY, and VA, and the countries of ALGERIA, AUSTRALIA, BELGIUM, BRAZIL, CANADA, DENMARK, FINLAND, FRANCE, GERMANY, GUADELOUPE, INDIA, INDONESIA, ISRAEL, ITALY, JAPAN,KOREA, LATVIA, MARTINIQUE, NETHERLANDS, NORWAY, PHILIPPINES,S POLAND, REUNION, ROMANIA, RUSSIA, SAUDI ARABIA, SINGAPORE, SOUTH AFRICA, SPAIN, SWEDEN SWITZERLAND, THAILAND, TUNISIA, TURKEY, UNITED KINGDOM, and VIETNAM.
GE Healthcare, Advantage Workstation, READY View Application.   Image analysis software.
GE Healthcare has become aware that when analyzing fMRI images using the READY View application software, incorrect fMRI activation maps may be computed and displayed.
Fresh Basil (Sweet Hawaiian and Thai)   New Dream Team Inc.  HI
6504 lbs of sweet basil (Hawaiian); 810 lbs of thai basil
State of HI issued Cease and Desist Order to grower of basil for positive sample results for pesticides not allowed on basil.
IBU (TM) IBUPROFEN Tablets, USP, 800 mg, 500 -count bottle,(NDC 55111-684-05) Rx only, Distributed by Dr. Reddy's Laboratories, Inc., Bridgewater, NJ  08807 USA.
Labeling: Incorrect or missing lot and/or exp date- This product is being recalled due to an incorrect expiration date of 05/2017. The correct expiration date is 10/2016.
Product was distributed to the following states: Virginia and Tennessee
Frozen,  4/3 lb unlabeled bags contained in a master carton box labeled in part: ''Portico Brand 4/3 lb 170585 Breaded Scallops***Net Wt 12 lb (5.44 kg)***Ingredients:Scallops, Bleached Wheat Flour, Water, Modified Corn Starch, Sugar, Yellow Corn Flour, Salt, Textured Soy Flour, Yeast, Dried Whole Eggs, Sodium Tripolyphosphate, Partially Hydrogenized Soybean Oil, Xanthan Gum, Sodium Hexametaphosphate. Contains: Wheat, Soy, Egg.''
Worldwide Distribution - USA (nationwide) including the states of : AL AZ, CA, CO, CT, FL, GA, IL, IN, MD,MI, MO, NJ, NY, NC, OK, PA, TX and WI., and the countries of :  AUSTRIA, BELGIUM, CANADA, FINLAND, FRANCE, GERMANY, GREAT BRITAIN, IRAQ, JAPAN, LEBANON, NORWAY, PORTUGAL, SPAIN, SWEDEN and TAIWAN.
GE Healthcare, Seno Advantage, 5183685, 5183685-2, 5183685-3, 5183685-4, 5183685-5, 5183685-6, 5183685-7, 5183685-8, 5183685-9, 5342425, 5342425-2, 5342425-3, 5342425-4, 5342425-5.   Seno Advantage is a medical image review station that allows easy selection, processing, filming and media interchange of multi-modality images from a variety of diagnosis imaging systems. When interpreted by a trained physician, mammographic images displayed on the high-resolution monitors may be used as an element for diagnosis. Furthermore filmed images from all modalities may also be used as an element for diagnosis.
GE Healthcare has recently become aware that patient mismatch without a warning message could occur on Seno Advantage (SA) workstations under certain circumstances. This issue may impact patient safety.
Meyer Lemon Braising Base, 1lb. 8.5 oz, 12 jars/case
Premier Foods is recalling Williams-Sonoma flavored sauces due to undeclared milk, soy (hydrolyzed soy protein), and wheat allergens.
40-Clove Garlic Chicken Braising Base, 24.5oz, 12 jars/case
Premier Foods is recalling Williams-Sonoma flavored sauces due to undeclared milk and wheat allergens.
Artichoke Pecorino Sauce, 16 fl. oz., 12 jars/case
Premier Foods is recalling Williams-Sonoma flavored sauces due to undeclared soy allergens (hydrolyzed soy protein).
USA Distribution in the states of  NH, MD, CO, and IL.
C2244.3808, CONELOG Titanium Base CC 3.8GH0.8 inkl HS   Product Usage:  Endosseous dental implant abutment CONELOG Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CONELOG implants to support prostheses in the maxillary and/or mandibular arch.
Product not cleared for sale/use in the United States.
C2244.3820;, CONELOG Titanium Base CC 3.8GH2.0 inkl HS   Product Usage:  Endosseous dental implant abutment CONELOG Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CONELOG implants to support prostheses in the maxillary and/or mandibular arch.
C2244.4308 CONELOG Titanium Base CC 4.3GH2 0.8 inkl HS   Product Usage:  Endosseous dental implant abutment CONELOG Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CONELOG implants to support prostheses in the maxillary and/or mandibular arch.
C2244.5008 CONELOG Titanbasis CAD/CAM Conelog  Titanium Base CAD/CAM  Rx only  5.0GH 0.8 inkl HS    Product Usage:  Endosseous dental implant abutment CONELOG Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CONELOG implants to support prostheses in the maxillary and/or mandibular arch.
Worldwide Distribution - USA (nationwide) including the states of : AL, AZ, AR, CA, CO, CT, FL, GA, ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MS, MO, NE, NV,NH, NH, NM, NY, NC, OH, OK OR, PA, PR, SC, TN, TX, VA, WA, WV, WI and  WY., and the countries of : ARGENTINA, AUSTRALIA, AUSTRIA, BAHRAIN, BANGLADESH, BELGIUM, BOLIVIA, BRAZIL, BULGARIA, CANADA, CHILE, COLOMBIA, COSTA RICA. CROATIA, CZECH REPUBLIC, DENMARK, EGYPT, FINLAND, FRANCE, GERMANY, HONG KONG, HUNGARIA, ICELAND, INDIA, INDONESIA, IRAQ, IRELAND, ISRAEL, ITALY, JAPAN, JORDAN, KOREA, KUWAIT, LEBANON, LITHUANIA, MALAYSIA, MOROCCO, NETHERLAND, NEW ZEALAND, NICARAGUA, NORWAY, OMAN, PAKISTAN, PANAMA, PARAGUAY, PERU, POLAND, PORTUGAL, QATAR, ROMANIA, RUSSIA, SAUDI ARABIA, SINGAPORE, SLOVAKIA, SLOVENIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, SYRIA, THAILAND, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM and VENEZUELA.
GE Healthcare, CARESCAPE Monitor B650.   The CARESCAPE Monitor B650 is a multi-parameter patient monitor intended for use in multiple areas and intra-hospital transport within a professional healthcare facility. The CARESCAPE Monitor B650 is intended for use on adult, pediatric, and neonatal patients and on one patient at a time. The CARESCAPE Monitor B650 is indicated for monitoring and recording of, and to generate alarms for, hemodynamic (including EGG, ST segment, arrhythmia detection, ECU diagnostic analysis and measurement, invasive pressure, non-invasive blood pressure, pulse oximetry, cardiac output, temperature and mixed venous oxygen saturation), impedance respiration, airway gases (C02, 02, N20 and anesthetic agents), spirometry, gas exchange, and neurophysiological (including electroencephalography, Entropy, Bispectral Index (HI1S) and neuromuscular transmission) status. The CARESCAPE Monitor B650 can be a stand-alone monitor or interfaced to other devices. It can also be connected to other monitors for remote viewing and to data management software devices via a network. The CARESCAPE Monitor B650 is intended for use under the direct supervision of a licensed healthcare practitioner, or by personnel trained in proper use of the equipment in a professional healthcare facility. The CARESCAPE Monitor B650 is not intended for use during MRI.
GE Healthcare has recently become aware of a number of  potential issues associated with the CARESCAPE Monitor B650.   No injuries or illnesses have been reported.
Worldwide Distribution - USA including AK, AR, AZ, CA, CO, DC, DE, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MT, , NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, TN, TX, UT, VA, WA, WI & WV.  Internationally to ARGENTINA, AUSTRALIA, AZERBAIJAN, BELGIUM, CANADA, CHILE, CHINA, COSTA RICA, CROATIA, GERMANY, HONDURAS, HONG KONG, INDIA, INDONESIA, ISRAEL, KOREA, KUWAIT, MEXICO, NEW ZEALAND, PERU, SAUDI ARABIA, SINGAPORE, SPAIN, TAHITI, THAILAND, THE NETHERLANDS, THE PHILIPPINES, UNITED ARAB EMERITES & UNITED KINGDOM.
Blanketrol III, Model Number 233, Cincinnati Sub-Zero Products, Inc., 12011 Mosteller Road, Cincinnati, OH 45241   Hyper-Hypothermia device used to lower or to raise a patients temperature and/or maintain a desired patient temperature through conductive heat transfer.
During a label review it was discovered that both the Blanketrol III Operations (57201-N) & Operations & Technical (56201-Q) manuals had verbiage added back into the manual during ECN M111-4260 (released 12/29/2011) which was previously removed for clarification of the intended use and subsequent 501(K) approval.
Worldwide Distribution-USA (nationwide) including the states of CA, CO, CT, HI, IL , IA, KY, LA, MA, MI, NE, NY,OH, OK, TX, and WI, and the countries of UNITED KINGDOM, UNITED ARAB EMIRATES, TURKEY, TUNISIA, THAILAND, SYRIAN ARAB REPUBLIC, SWITZERLAND, SWEDEN, SPAIN, SOUTH AFRICA, SLOVAKIA, SINGAPORE, SAUDI ARABIA, RUSSIAN FEDERATION, REPUBLIC OF SERBIA, PORTUGAL, POLAND, PARAGUAY, NORWAY, NETHERLANDS, NEPAL, MEXICO, MALAYSIA, KUWAIT, REPUBLIC OF KOREA, JORDAN, JAPAN, ITALY, ISRAEL, IRELAND, IRAQ, INDONESIA, INDIA, HONG KONG, GREECE, GERMANY, FRANCE, FINLAND, ESTONIA, EGYPT, DENMARK, CZECH REPUBLIC, COSTA RICA, COLOMBIA, CHINA, CHILE, CANADA, BOSNIA AND HERZEGOVINA, BELGIUM, BAHRAIN, AUSTRIA, and AUSTRALIA.
GE Healthcare, CARESCAPE Monitor B850.   Intended for use in multiple areas within a professional healthcare facility.
GE Healthcare has recently become aware of an issue associated with the CARESCAPE Monitor B850 when used with the iCentral network.  The iCentral must have the alarm management software license (L-NETM-00) and the alarm limit change option enabled to experience this issue.     When changing the HR, SpO2 or Invasive pressure alarm limits from the iCentral over the network, the alarm priority on the CARESCAPETM Monitor B850 inadvertently changes from Escalating to the startup level of the escalation (e.g., low for HR Alarms). Alarms for other parameters are not affected.
Vicks NyQuil Cold and Flu Nighttime Relief, Liquid Twin Pack, (Acetaminophen 650mg,  Dextromethorphan HBr 30mg, Doxylamine succinate 12.5mg), 12 fl oz (354 ml) bottles, Distributed by Procter & Gamble, Cincinnati, OH 45202,  NDC 37000-807-12
Lot #s  31614334R1, 31814334R1, Exp 5/15;  Twin packs were further packaged in display coded with following 4 Lot #s (display received by WalMart only): 3051A152HK, Exp 1/15, 3051A152HL, Exp. 1/15, 3051A152HM, Exp 1/15, 30746493F5, Exp 2/15
Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were inadvertently overwrapped with NyQuil Liquid Cherry information as a result the outer wrap does not correctly identify color additives, particularly FD&C Yellow No. 6 and FD&C Yellow 10.
Worldwide distribution: US (nationwide) including states of : PA and TN; countries of: FRANCE and SINGAPORE.
GE Healthcare Discovery IGS 730 Cardiovascular X-Ray Imaging System.   The angiography X-ray systems are indicated for use in generating fluoroscopic and rotational images of human anatomy for cardiovascular, vascular and non-vascular, diagnostic and interventional procedures. Additionally, with the OR table, the angiographic X-ray systems are indicated for use in generating fluoroscopic and rotational images of human anatomy for image guided surgical procedures. The OR table is suitable for interventional and surgical procedures.
GE Healthcare has recently become aware of a potential safety issue with respect to Discovery IGS 730 Imaging Systems.   A patient data management error may prevent the Discovery IGS 730 Imaging System from booting on start-up or re-booting during procedure. The boot issue may occur when a large  amount of patient data remains in the browser and is not deleted. The inability to boot the system may lead to a complete loss of real-time interventional imaging functionality.  No injuries have been reported due to this issue.
Hydrocodone Bitartrate and Acetaminophen Tablets, 7.5 mg/650 mg Tablets, 500 Count Bottle, Manufactured by: Watson Laboratories, Inc, Cocona, CA 92880, NDC 0591-2611-05.
Defective Container:  Defective bottles may not have tamper evident seals properly seated, and therefore it may be difficult to determine if the product had been opened or tampered with.
Testosterone Cyp 200 mg/mL, W/Pres. (Benzyl ETOH), 3 mL, Medaus pharmacy 1-800-526-9183
Lipo-Injection w/ Lidocaine (PF), Ascorbic Acid 50 mg; B1-50 mg; B2-5-PO4-5 mg; B3-50 mg; B5-5 mg; B6-5 mg; Cyano B12-100 mcg; Methionine 12.5 mg; Inositol-25 mg; Choline-25 mg; Lidocaine 10 mg/mL, 30 mL, Medaus Pharmacy 1-800-526-9183
Taurine 50 mg/mL PF, 100 mL, Medaus Pharmacy 1-800-526-9183
L-Glutathione 200 mg/mL PF, 100 mL, Medaus Pharmacy 1-800-526-9183
Pyridoxine HCL 100 mg/mL NS (PF), 30 mL, Medaus Pharmacy 1-800-526-9183
Magnesium Chl 200 mg/mL PF, 100 mL, Medaus Pharmacy 1-800-526-9183
NA Ascorbate 500 mg/mL, PF, 100 mL, Medaus Pharmacy 1-800-526-9183
NA Ascorbate 500 mg/mL, non corn PF, 100ML, Medaus Pharmacy, 1-800-526-9183
Distributed in the states of California, Idaho, Oregon, and Washington.
Zeppessis' reprocessed single-use manifolds (filters) for the Stryker Neptune 1 and Neptune 2 Waste Management Systems:   The Neptune Waste management system is intended to be used in the Operating Room, Surgical Centers and Doctor's Offices to collect and dispose of surgical fluid waste as well as collect smoke generated from electrocautory or laser devices. ***The single-port manifold for the Stryker Neptune 1 (part # 700-015-000) can be used with the: Neptune 1 Gold Rover or the Neptune Bronze Rover as an accessory to Class 2 Air-handling apparatus for a surgical operating room (Sec. 878.5070); or with the Neptune 1 Silver Rover as an accessory to Class 2 Powered suction pump. ***four-port manifold for the Stryker Neptune 1 (part # 700-020-000) can be used with the: Neptune 1 Gold Rover or the Neptune Bronze Rover as an accessory to Class 2 Air-handling apparatus for a surgical operating room (Sec. 878.5070); or with the Neptune 1 Silver Rover as an accessory to Class 2 Powered suction pump. ***single-port manifold for the Stryker Neptune 2 (part # 702-025-000) can be used with the Neptune 2 Rover Ultra as an accessory to Class 2 Powered suction pump. ***four-port manifold for the Stryker Neptune 2 (part # 702-020-000) can be used with the Neptune 2 Rover Ultra as an accessory to Class 2 Powered suction pump.
-Single-port manifold for the Stryker Neptune 1 (part # 700-015-000); -Four-port manifold for the Stryker Neptune 1 (part # 700-020-000);   -Single-port manifold for the Stryker Neptune 2 (part # 702-025-000);   -Four-port manifold for the Stryker Neptune 2 (part # 702-020-000).
Zeppessis' reprocessed single-use manifolds (filters) for the Stryker Neptune 1 and Neptune 2 Waste Management Systems are recalled due to lacking 510K and and without a validated cleaning protocol for reprocessing the used manifolds.
King LT-D Oropharyngeal Airways Class 1, 510(k) exempt    The King LT-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.
King Systems is initiating a voluntary recall of an affected lot of its KLTD products shipped on April 30, 2013. King Systems has received a report that size 5 KLTD airways were packaged in pouches indicating a size of 2.5 and shipped to your facility. The correct size of the KLTD airway is clearly marked on the actual airway product and the physical size difference between 2.5 and 5 is distinct and obvious.  King Systems has received no reports of serious injuries or deaths resulting from this issue.
Integra LifeSciences Corp. d.b.a. Integra Pain Management
Nationwide Distribution including CA, CO, FL, IN, KS, NC, NV, NY, OK, TN, TX, VA, WA, and WI.
Cranial Access (CRAK) Kits, Product / Catalogue No.s: INSHITH, INSHITHND, INSHITHRZN   The kits allow for access to the subarachnoid space or the lateral ventricles of the brain. The kits are intended to be used with an external drainage and monitoring system in selected patients to reduce intracranial pressure (ICP), to monitor CSF, to provide temporary drainage of CSF, and to monitor ICP.
Integra is recalling certain lots of Cranial Access Kit due to a possibility that the seal integrity of the sterile package may become compromised during shipping.
AL, AZ, CA, CO, CT, FL, GA, IL, IN, KY, MA, MD, ME, MS, MT, NC, NH, NJ, NY, NM, OH, PA, RI, SC, TN, VA, WY
Olde Cape Cod Chipotle Ranch dressing, 16 oz.  Item Number:  90997-11630
Product may be labeled with an incorrect back panel label that does not declare the allergens milk and egg.
Northern New England Compounding Pharmacy LLC
Hydroxocobalamin MDV 5 mg/mL (5,000 mcg/mL) Inj., 10 mL vial X 3, Eastern States Compounding Pharmacy, Littleton, NH 03561
Lack of Assurance of Sterility: The pharmacy is recalling one lot of Hydroxocobalamin MDV 5mg/mL due to failed sterility results by a third party contract testing lab. Hence the sterility of the product cannot be assured.
Worldwide Distribution - USA Nationwide in the states of MA, CT, NJ, DE, NY, FL, OK, TX, PA, DC, IL, KS, LA, MD, CA, RI, TN, MN, and SC and the countries of  Canada, Japan, Australia, Italy Germany, France, Switzerland, Apain, Brazil, Uruguay, Singapore, Dominican Republic, Taiwan, Austria, Portugal, and the United Kingdom.
Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm (L) Dental Implant   Product Usage:  Surgical placement in the upper or lower jaw to provide a means for prosthetic attachment in single tooth restorations and in partially or fully edentulous spans with multiple single teeth utilizing delayed or immediate loading or with a terminal or intermediary abutment for fixed or removable bridgework and to retain over dentures.
One of the dental implants do not have the internal hex feature.  One of the dental implants do not have the internal thread feature.
Osseotite Parallel Walled Certain 4mm(D)X 15mm (L) Dental Implant   Product Usage:  Surgical placement in the upper or lower jaw to provide a means for prosthetic attachment in single tooth restorations and in partially or fully edentulous spans with multiple single teeth utilizing delayed or immediate loading or with a terminal or intermediary abutment for fixed or removable bridgework and to retain over dentures.
Worldwide distribution: US (nationwide) including states of NY, KY, and CO, and the country of Israel.
Device Name: Terino Square Chin-Style II-Medium; Catalog Number: TSCII-M.   To augment or reconstruct underdeveloped or traumatized mandibular region.
Catalog Number: TSCII-M Lot Numbers: 848488 and 850156
Implantech initiated a voluntary recall of certain lots of Terino Square Chin-Style II-Medicum (Lot # 848488 and 850156), after determining that the devices from the lot numbers do not conform to the dimensional requirements for the TSCII-M.
Bevacizumab 1.25 mg/0.05 mL PF, Avella Specialty Pharmacy, Phoenix, AZ, 85085, 877-782-7684
Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling bevacizumab and vancomycin due to concerns of sterility assurance with the specialty pharmacy's independent testing laboratory.
Vancomycin PF (BSS) 1%, 1 mL, Avella Specialty Pharmacy, Phoenix, AZ 85085, 877-782-7684
AL, AZ, AR, CA, CO,CT, FL, GA, ID, IL, IN, KS,KY, LA, ME, MD,MA, MI, MN, MS,MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WY.
Pills bury Cinnamon Rolls with Icing, CINNA BON, USPC 1800000501, 1800052230, 12.4 oz  and 2-pack USPC 1800045675,2- 12.4 oz (351 G) CANS, NET WT 24.8 OZ (1 LB 8.8 OZ 703 G.
Better if Used Date on Package:   30OCT2013, 31OCT2013, 18OCT2013, 26OCT2013 and 31OCT2013.
General Mills is recalling a limited quantity of refrigerated Pills bury Cinnamon Rolls with Icing.  The dough may contain fragments from a broken piece of plastic on the production line.
POWERWAND Safety Introducer with Extended Dwell Catheter; Catalog no. 92006.    Used to gain access to the vascular system to sample blood and administer fluids intravenously.
Access Scientific is recalling the POWERWAND Saftey Introducer with Extended Dwell Catheter because it is mislabeled.
Product was shipped to one manufacturer in MN.
Bean & Cheese Burrito Filling, 10 lb bags Labeled in part ''13210 B 1 77220 13:38 KEEP FROZEN BEAN & CHEESE BURRITO FILLING***INGREDIENTS: COOKED PINTO BEANS, WATER, CHEDDAR CHEESE***SOYBEAN OIL***STARCH-MODIFIED, ONIONS, CHEESE SAUCE BASE***CONTAINS LESS THAN 2% OF CHILI PEPPER, SALT, CHICKEN BASE***SODIUM PHOSPHATES, SPICE, CARAMEL COLOR DEHYDRATED, GARLIC, ANNATTTO EXTRACT.''  CONTAINS: Soy, Milk, Wheat JTM Food Group 200 Sales Dr. Harrison, OH 45030 Phone 800.626.2308.
Undeclared eggs in the product.  The firm was notified by their customer that the product contains pasta.  The pasta contains eggs which is not declared on the label.
Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical
Worldwide Distribution, including Nationwide in the US and the countries of Canada, Great Britain, Australia, France, Germany, Italy, Denmark, Hong Kong, China, Brazil and Saudi Arabia.
NX3 Try-In Gel. The product is used as a tooth shade resin material.
Part Number 33660. Syringe Lot Number 4580333.  Autobag Lot Number 4584609.
Kerr Corporation is voluntarily recalling one lot of NX3 Try-In Gel, because some of the NX3 Try-In Gel syringes in the affected lot contain a different product material. The material in the affected syringe does not match the shade of the cement as it is labeled.