Blood products, collected from a donor who was at risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.
Blood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.
Red Blood Cells (Apheresis) Leukocytes Reduced
Blood and Blood Products for Reprocessing
Blood products, collected from a donor who received a body piercing within 12 months of donating, were distributed.
Blood product, collected from a donor who reported travel to a malarial endemic area, was distributed.
Blood product, labeled as leukoreduced without the assurance that it met the criteria for a leukoreduced product, was distributed.
Blood product, stored at an unacceptable temperature, was distributed.
Blood product, collected from a donor whose suitability to donate was not adequately determined, was distributed.
Blood products, collected from donors whose arm scrubs were performed using expired cleanser, were distributed.
Blood product, collected from a donor whose donor suitability was not adequately determined, was distributed.
Red Blood Cells Leukocytes Reduced Irradiated
Blood product, exposed to unacceptable shipping temperatures, was distributed.
Blood component, processed from Whole Blood stored at room temperature for more than 8 hours after collection, was distributed.
Blood products, collected from a donor whose suitability to donate was not adequately determined, were distributed.
Blood product, collected from a donor who did not respond to questions regarding increased risk for vCJD, was distributed.
Blood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Blood products, collected from a donor who received a tattoo within 12 months of donating, were distributed.
Blood products, collected from a donor who may have received a body piercing within 12 months of donating, were distributed.
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Red Blood Cells Leukocytes Reduced Washed
Blood product, for which the red cell count and hematocrit were outside the acceptable range, was distributed.
Blood products, collected from donors for whom donor suitability was not adequately determined, were distributed.
Platelets Pheresis Leukocytes Reduced Irradiated
Blood products, collected from a donor with a history of high-risk behavior, were distributed.
Blood products, for which the scale and Hemocue used during collection failed quality control testing, were distributed.
Worldwide Distribution: USA (nationwide) including states of: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY; and CANADA LOCATIONS: AB, BC, MB, NB, NS, ON, and SK.
Liko Overhead Rail System   Product Usage - The Overhead Rail System allows overhead lifts to be mounted to the ceiling allowing versatility for use in lifting situations. It can be used with different Liko ceiling lifts.
The Liko Overhead Rail System components are not serialized and have been distributed since the early 1980's to the present.
Liko/Hill-Rom to date has received two reports from facilities alleging that the overhead rail system has failed to the extent that the overhead rails have fallen down while in use in high humidity (swimming pool) areas.  Analysis of the incidents suggest that the components (hardware) used to secure the rail to the ceiling had corroded and may be unsuitable for environments with an atmosphere containing chlorine.
Stryker Sustainability Solutions, AC Power Adaptor for Restep Deep Vein Thrombosis (DVT) System, an external compression system.   PUMPKIT (Pump Kit), and RSP159-01 - AC Power Adaptor.
Reports that the AC Power Adaptor may not operate due to wires coming loose in the unit.
Worldwide Distribution - US Nationwide in the states of AL, AZ, CA, CO, FL, GA, ID, IL, MA, MD, MI, MN, NC, NM, NV, NY, OH, PA, SC, SD, TN, TX, VA, WA, WI, and WV and the countries of Holland, Australia, Austria, South Africa and Canada including Veteran Administration hospitals.
LPS Diaphyseal Sleeves   Product Usage:  The LPS Diaphyseal Sleeves are used with the LPS System which is an end-stage revision knee product that allows surgeons to reconstruct severe soft tissue and bony defects.
162 total units (US) and 102 units total (OUS)
DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal sleeve because the product has the potential for fracture at the taper junction. The LPS Diaphyseal Sleeve to Diaphyseal Sleeve Base taper connection may not be sufficient to accommodate potential physiologic loads that may be transferred to the junction during normal gait activities by some patients.
Mylan Institutional, Inc. (d.b.a. UDL Laboratories)
Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 10 mg/500 mg; 100 Tablets (5 x 20), 5 cards each containing 20 blistered tablets per carton, Rx only; Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, Pkg by &amp;amp; Distributed by UDL Laboratories, Inc., Rockford, IL 61103; NDC 51079-254-21.
Superpotent (Multiple Ingredient) Drug: Oversized tablets resulting in superpotent assays of both the hydrocodone and acetaminophen components.
CA, CO, FL, GA, NC, NJ, OH, TX, and WI.  No international distribution.
HealthTronics Endocare 3.8mm RenalCryo Cryoprobe, R3.8L, Endocare, Inc., a wholly owned subsidiary of HealthTronics, Inc., 9825 Spectrum Dr. Building 3, Austin, TX 78717   The Endocare CryoProbe is an accessory probe intended for use with the CryoCare Surgical System. The CryoCare Surgical System is intended for use in surgical procedures in the arrears of general surgery, dermatology, neurology, thoracic surgery, pulmonary surgery,
Lot 10180, Expiration date on box is 2105-07.  Model Number R3.8L
The Endocare 3.8mm RenalCryo Cryoprobe is being recalled because the label on the outer box has the incorrect expiration date.
SLIMDIA Revolution capsules, 30-count capsules per bottle, Yerba Naturals, 19685 Varda Ave., Buena Park, CA.
There are no manufacturing codes associated with the product.
Marketed Without an Approved NDA/ANDA: All lots of the dietary supplement Slimdia Revolution are being recalled because they contain sibutramine, a previously approved FDA drug removed from the U.S. marketplace for safety reasons, making it an unapproved new drug.
Worldwide Distribution - USA (nationwide) and Internationally to Bermuda, Canada, Chile, Denmark, Germany,Italy,Latvia, Lithuania, Malaysia, Phillipines, South Africa, Spain, Switzerland, Taiwan, and United Arab Emirates.
Pro Time Microcoagulation System/ Pro Time 3 Cuvette International Technidyne Corporation 23 Nevsky Street Edison, NJ 08820    The Pro Time Microcoagulation System is a portable batter operated instrument with a disposable cuvette for quantitative determination of prothrombin time from fingerstick whole blood or anticoagulant free venous whole blood.
11742 boxes US (25 cuvettes per box); 22,968 boxes OUS (25 cuvettes per box)
Some Pro Time3 Test Cuvettes within a specified lot range may recover lower than expected Prothrombin Time/International Normalized Ratio (PT/INR) results.
Crest PRO-HEALTH CPC Antigingivitis/Antiplaque Oral Rinse, 250 mL (8.4 fl oz),Dist.  by Procter & Gamble, Cincinnati, OH 45202  NDC 37000-452-02
Cross Contamination with Other Products: Product was mixed with another type of mouth wash.
Worldwide Distribution - USA (nationwide) and Internationally to Austria, Belgium, Canada, Chile, Costa, Rica, Czech Republic, Denmark, France, Germany, Great Britian/UK, Ireland, Italy, Lithuania, Malaysia, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovakia, Spain, and Switzerland.
NEUROPATH 6Fx90 GUIDING CATH MPC Product Code: GMC60900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
Sterility of device may be compromised due to lack of  packaging integrity
NEUROPATH 5Fx90 GUIDING CATH S2 Product Code: GSM50900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
Sterility of device may be compromised due to lack of package integrity
NEUROPATH 6Fx90 GUIDING CATH HH Product Code: GHH60900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GHH51000000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GMC51000000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 6Fx100 GUIDING CATH MPD Product Code: GMD60900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 5Fx100 GUIDING CATH MP Product Code:GMD51000000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 6Fx100 GUIDING CATH ST Product Code: GST61000000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 5Fx100 GUIDING CATH S2 Product Code: GSM51000000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 6Fx100 GUIDING CATH MC Product Code: GCB61000000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 6Fx100 GUIDING CATH S2 Product Code: GSM61000000     Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 5Fx100 GUIDING CATH MC Product Code: GCB51000000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 5Fx90 GUIDING CATH MCV Product Code: GCB50900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 5Fx90 GUIDING CATH MPC Product Code: GMC50900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMD61000000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 5Fx90 GUIDING CATH MPD Product Code: GMD50900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 5Fx100 GUIDING CATH ST Product Code: GST51000000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 5Fx90 GUIDING CATH ST Product Code: GST50900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 6Fx90 GUIDING CATH ST Product Code: GST60900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 5Fx90 GUIDING CATH HH Product Code: GHH50900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 6Fx90 GUIDING CATH MCV Product Code: GCB60900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 6Fx90 GUIDING CATH S2 Product Code: GSM60900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 6Fx100 GUIDING CATH HH Product Code: GHH61000000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMC61000000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
Worldwide Distribution - USA including AL, AR, AZ, CA, CO, CT, FL, GA, IL, IN, KY, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NM, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA & WI.  Internationally to Belgium.
MAYFIELD Composite Series  Base Unit Standard, Model (A3101), Rx ONLY, Integra LifeScience Corporation, 4900 Charlemar Drive, Building A, Cincinnati, OH 45227   The MAYFIELD Base Units are intended to be used to support a patient during diagnostic examination and/or surgical procedures where a rigid support between surgical table and headrest, or skull clamp is necessary, positional freedom is required and where X-ray imaging modalities will be used.
Integra determined there is a possibility that the Base Units may break during use.
Products were to distributed to grocery outlets within the US in AL, FL, GA, LA, MS, NC, SC, and TN.
Thomas' Bagels, 1 lb 4 oz packages; EVERYTHING, ONION, BLUEBERRY, PLAIN, CINNAMON RAISIN, HEARTY GRAINS 100% WHOLE WHEAT, CINNAMON SWIRL and HONEY WHEAT varieties.
Best buy dates (month and day) ''JAN 18'' to and including ''JAN 27'' found on the lock tab bag closures in the following states:  AL, FL, GA and TN.
The firm found metal fragments in two packages of product.
Sara Lee Deluxe Bagels, 20 oz packages; BLUEBERRY,  PLAIN, CINNAMON RAISIN,and HONEY WHEAT varieties.
Best buy dates (month and day) ''JAN 18'' to and including ''JAN 27'' found on the lock tab bag closures in the following states:  AL, FL, GA, LA, MS, NC, SC and TN.
Publix Premium Bagels, 20 oz packages; ORIGINAL, MULTI-GRAIN, and CINNAMON RAISIN SWIRL varieties.
Best buy dates (month and day) ''JAN 18'' to and including ''JAN 27'' found on the lock tab bag closures in the following states:  AL, FL, SC and TN.
Weight Watchers 6 Original Bagels, 15 oz packages
Best buy dates (month and day) ''JAN 18'' to and including ''JAN 27'' found on the lock tab bag closures in the following states:  AL, FL, GA, NC, SC and TN.
Blood product, collected from a donor with an initially positive test for syphilis, was distributed.
Worldwide Distribution - USA (nationwide) and Internationally  to ALGERIA, ANGOLA, AUSTRALIA, AUSTRIA, BAHRAIN, BELGIUM, BULGARIA, COLOMBIA, CROATIA (LOCAL NAME HYVATSKA), CYPRUS, CZECH REPUBLIC, DENMARK, DOMINICAN REPUBLIC, EGYPT, ESTONIA, FINLAND, FRANCE, GABON, GERMANY, HONG KONG, HUNGARY, ICELAND, INDIA, INDONESIA, IRAN (ISLAMIC REPUBLIC OF), IRAQ, IRELAND, ISRAEL, ITALY, JORDAN, KENYA, REPUBLIC OF KOREA, KUWAIT, LATVIA, LEBANON, LIBYAN ARAB JAMAHIRIYA, LITHUANIA, MALAYSIA, MALTA, MAURITIUS, MOROCCO, NAMIBIA, NETHERLANDS, NEW ZEALAND, NORWAY, OMAN, PALESTINE, POLAND, PORTUGAL, ROMANIA, SAUDI ARABIA, SINGAPORE, SLOVAKIA (SLOVAK REPUBLIC), SLOVENIA, SOUTH AFRICA, SPAIN, SRI LANKA, SWEDEN, SWITZERLAND, SYRIAN ARAB REPUBLIC, TANZANIA, THAILAND, TRINIDAD AND TOBAGO, TUNISIA, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM, AND VIET NAM.
Philips HeartStart XL+ Defibrillator/Monitor  Model number: 861290    The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or defibrillation
Philips HeartStart XL+ Defibrillator/Monitor may become locked out of clinical use
Worldwide Distribution - USA including the states of   NJ, FL, GA, MO, AZ, UT and the country of  Denmark
Merit Medical Systems Inc.,  Resolve Biliary Locking Drainage Catheter, Models RBC and RBDC, used for drainage of bile within the biliary system.
Merit Medical Systems is recalling certain lots of ReSolve Biliary Locking Drainage Catheters due to a consumer complaint that a catheter was observed to be in several pieces under patient fluoroscopic visualization.
Nationwide Distribution including the states of  AK, CA, CO, IL, MO, NV, NY, TX and UT.
CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer blood and blood products through a needle or catheter inserted into the patient's artery or vein.
CareFusion is recalling the SmartSite Gravity Blood Set as a result of a potential for separation at the connection of the drip chamber and tubing . The separation may be observed at priming or observed during use. If a separation between the drip chamber and tubing occurs, this could cause a delay in treatment.
Human Tissues, recovered from a donor whose donor eligibility determination did not identify if the donor was free from risk factors for and clinical evidence of, infection due to relevant communicable disease agents, were distributed.
Worldwide Distribution - USA Nationwide including the states of AL, AZ, AR, CA, CO, CT, DE, CD, FL, GA, HI, ID, IL ,IN, IA, KY, LA, ME, MD, MA, MI,MN, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, SC, SD, TN, TX, UT, VT VA, WA, WV, WI, WY and AUSTRIA, CANDA, DENMARK, FINLAND, FRANCE, GERMANY, GREECE, HUNGARY, ISRAEL,. ITALY, MEXICO, NETHERLANDS, NORWAY, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, TURKEY, UNITED KINGDOM.
Vascular Solutions, SuperCross Microcatheter, Sterilized using ethylene oxide, Rx Only, Model numbers 5300 - 5307, 5324, 5325, 5329, 5332, 5336, 5340, and 5341.   Product Usage:  The SuperCross catheter is intended to be used in conjunction with steerable guidewires to access discrete regions of the coronary and/or peripheral vasculature. It may be used to facilitate placement and exchange of guidewires and other interventional devices and to subselectively infuse/deliver diagnostic and therapeutic agents
Vascular Solutions, Inc has discovered a potential problem with a number of lots  of Supercross microcatheters. A potential for surface contamination on aged catheters was observed during in-house testing.
Human Corneas, recovered in a manner that increased the risk of the introduction, transmission, or spread of communicable disease, were distributed.
A soft brie-style cheese called Jewell. Ingredients:  Certified organic cows' milk, Pasteurized farmstead goats' milk, cultures, rennet and salt. (information obtained from firm's web site)
Packages are labeled with a ''born on date'' along with the weight of the package.  The cheeses range in weight.  The package also contains a packaged date which represents the date shipped.
A soft chevre-style cheese. Label reads in part, ''*** TUMALO FARMS Artisan Cheeses of Central Oregon Chevita This fresh and mild, soft, white cheese has a great tangy finish www.tumalofarms.com *** Ingredients . Pasteurized Goats' Milk, Culture, Rennet and Salt.''
Product is coded with a ''born on date'' and weight (individual cheese packages are different weight.  The product also has a packaged date, which is the same as the ship date.  there are 2 born on dates - 1/10/13 and 1/24/13
From production date 1/10/13 10 - 4 oz tubs and 4-2 lb tubs; from production date 1/24/13 3 4 oz tubs and 8 2 lb tubs
.Nationwide Distribution including the states of AL, AZ, CA, CO, DE, FL, GA, IA, IN, IL, KS, KY, LA,  MI, MN, MO.MS, NC, NH, NJ, NY, OH, OR, PA, RI, SC, TN, TX, VA, WI and UT.
LifeStyles ZERO 10 uber-thin lubricated latex condoms.  Mfd. for Ansell Healthcare Products LLC, Dothan, AL 96303.   A sheath which completely covers the penis with a closely fitting membrane. The condom is used for contraceptive and for prophylactic purposes (preventing transmission of sexually transmitted infections).
Out of an abundance of caution, Ansell is implementing a voluntary recall of the Zero Latex Condom (regular) product.  The condom has met or exceeded test and quality standards required by the Food and Drug Administration.  However, we are experiencing a number of complaints concerning the difficulty in unrolling and subsequent breakage, and so we are asking to have all products returned.
Worldwide Distribution-USA (nationwide) and the countries of China, Dubai and Indonesia.
ELECTROLASE HYFRECATOR(R) ELECTRODES - SHARP, REF/Catalog Number 7-100-8BX, Disposable Hyfrecator(R) Tips, Sterile, Rx Only --- CONMED CORPORATION 525 FRENCH RD., UTICA, NY 13502-5994 USA.   Intended to be used as active RF electrodes for desiccation, fulguration and coagulation.
Beginning Lot Code 120628X, Ending Lot Code 120917X. [Lot codes on boxes and packaging contain a lot code in the following format: 120917X where 12 represents the year (2012), 09 represents the month (September), 17 represents the day of the month, and X represents the manufacturing shift code (1, 2, 3, 4,5,6 or 9)].
Domestic Distribution:  97,450 units; Foreign Distribution: 6,800 units
ConMed received complaints of some devices which had broken through the seal of the sterile pouch.  ConMed confirmed instances where the pouch seal was compromised on the affected products.
ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT, REF/Catalog Number 7-101-8BX, Disposable Hyfrecator(R) Tips, Sterile, Rx Only --- CONMED CORPORATION 525 FRENCH RD., UTICA, NY 13502-5994 USA.   Intended to be used as active RF electrodes for desiccation, fulguration and coagulation.
Worldwide Distribution-USA including the states of AZ, CO, FL, TN, and TX and the countries of Australia, Canada, Czech Republic, Dubai/Bahrain/Kuwait/Lebanon/Saudi Arabia/Yemen, France, Germany, Hong Kong, Italy, Japan, Netherlands, Singapore, South Africa, Sweden, Switzerland, Thailand, Turkey, and UK.
Maquet ELS Cannula 15 FR. Used for extracorporeal membrane oxygenation (ECMO) for the treatment of respiratory insufficiency in infants.
41 units - US Distirbution; 216 units - OUS Distribution
ELS 15 Fr Cannula could potentially contain an occluded arterial lumen.
Worldwide Distribution-USA (nationwide) including Washington, DC, Puerto Rico, US Virgin Island and the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY, and the  countries of Austria, Australia, Bermuda, Canada, New Zealand, Czech Republic, Italy, France, Finland, Hungary, Israel, United Kingdom, Spain, Sweden, Norway, Denmark, Germany, Mexico and Ireland.
Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous subcutaneous infusion of insulin.
Due to an internal calendar date limit (December 31, 2015) these pumps will cease to operate on January 1, 2016, and will result in a call service alarm that is displayed on the pump display.
Varian Medical Systems, Inc. Oncology Systems
Varian Eclipse Treatment Planning System for Radiotherapy; Model Number: H48. In addition, the Eclipse Proton Eye algorithm is specifically indicated for planning proton treatment of neoplasms of the eye.
Varian has identified an anomaly with the Eclipse Treatment Planning (for radiotherapy treatments) where the calculation of dose dynamic plans containing different energy fields is incorrect when the Pencil Beam Convolution 11.0 algorithm (PBC 11.0) is used.
US Nationwide Distribution in the states of FL, IL, KY, NY, NC, PA, OH, TX, VA
VACUETTE Safety Blood Collection Set + Luer Adapter, 23x12'' Safety Blood Collect LA Product, Item number 450096.  Usage: The Safety Blood Collection Set is used in routine venipuncture procedures.
The VACUETTE Safety Blood Collection Set + Luer Adapter may display leaking (small droplets) during use due to a crack on the luer connector piece.
Nationwide Distribution-including the states of AK, CA, FL, NJ, NC, OH, OR, TN, TX, WA, and WI.
Monaco RTP System.   Radiation treatment planning.
The beam is displayed at the ''gantry'' angle, but the dose is calculated at the ''rotation_start'' angle.
Worldwide Distribution including  USA nationwide.
MEDRAD Hand Controller Sheath, Catalog number AVA 500 HCS/3010903, for cardiac catheterization procedures.  The Sterile Sheath is specifically intended for use in the x-ray angiography environment to cover the Medrad Avanta Sterile Hand Controller to prevent cross contamination between  patients.
Bayer is initiating this recall because in certain packages within the affected lots, the seal between the white polyethylene and the clear plastic may be missing on the Hand Controller Sheath package, resulting in a potential breach of the sterility of this accessory.
Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MI, MN, MO, MS, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI & WY.
Lean Cuisine Culinary Collection Mushroom Mezzaluna Ravioli ravioli filled with portobello & button mushrooms, romano & ricotta cheeses in a creamy marsala wine sauce with spinach & red peppers no preservatives, NET WT 8 5/8 oz (244g) 0 13800 58358 1 DISTRIBUTED BY: NESTLE' USA, INC., SOLON, OH 44139
Lot 2311587812 Best Before Dec2013 and Lot 2312587812 Best Before Dec2013, UPC Code 13800-58358
The firm received complaints of small fragments of glass that were found inside the ravioli portion of the entre.