Worldwide Distribution-USA including the states of AR, KS and OH, and the countries of Germany, South Africa and the United Kingdom.
The product is labeled in part ''***Surgical Laser Technologies, Inc. Montgomeryville, PA***SLT Fiber Delivery System***Sterile***Non-Pyrogenic***.     The product is packaged in a flexible pouch and includes the following laser surgery accessories - SLT-SSRH 8, Catalog/Product Number 0041-3082; SLT-SSRH 11, Catalog/Product Number 0041-3112; SLT-SSRH 4-SMA, Catalog/Product Number 0042-0075; SLT-SSRH 5-SMA, Catalog/Product Number 0042-0076; SLT-SSRH 6-SMA, Catalog/Product Number 0042-0077; SLT-SSRH 7-SMA, Catalog/Product Number 0042-0078; SLT-SSRH 8-SMA, Catalog/Product Number 0042-0079; SLT-SSRH 9-SMA,  Catalog/Product Number 0041-4931; and SLT-SSRH 10-SMA, Catalog/Product Number  0042-0081.    Indicated for the incision, excision, coagulations, and vaporization of soft tissue.
Firm became aware that some products within the specified lot may not have been sealed appropriately, thus compromising the sterile barrier.
Nationwide distribution: US including states of:  CA, GA, IN, KY, MO, NY, OR, TX, and WI.
Solitaire-35 Peek Solitaire Anterior Spinal System. The Solitaire-35 is an intervertebral body fusion device.
Several complaints were recorded regarding one of the three screws driving through the cage of the Solitaire 35 implant.
Product was distributed nationwide and included military distribution.  Foreign distribution was made to Panama and Belize.
Benefiber Fiber Supplement, Orange Natural Flavor, Non-Thickening Powder, Sugar Free, packaged in 5.7-oz. (35 servings) bottles, UPC 300670068356, 9.4-oz (58 servings) bottles, UPC 300670068585, and 18.7-oz. (115 servings) bottles, UPC 300670068158.   Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622, Made in France.
The products are being recalled due to the receipt of a relatively high number of consumer complaints.
Benefiber Plus Heart Health Non-Thickening Powder, Sugar Free, packaged in 6.4-oz (48 servings) bottles, UPC 300673002487.   Distributed by: Novartis Consumer health, Inc., Parsippany, NJ 07054-0622.  Made in France.
Benefiber Fiber Drink Mix, Cherry Pomegranate, Sugar Free, packaged in 5.0-oz. boxes containing 24/0.21-oz. stick packs,   UPC 300670107246.  Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622.  Made in France.
Benefiber Fiber Drink Mix, Kiwi Strawberry, Sugar Free, packaged in 5.0-oz. boxes containing 24/0.21-oz. stick packs, UPC 300670106249.   Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622.  Made in France.
Benefiber Fiber Supplement Plus Calcium, Orange Natural Flavor, Sugar Free, packaged in 10.76-oz (48 Servings) bottles,  UPC 300670108489.   Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622.  Made in France.
Benefiber Non-Thickening Powder, Sugar Free, packaged in the following configurations:   (1) 2.8-oz. (20 servings) bottles, UPC 300670044206;     (2) 4.6-oz. (32 servings) bottles, UPC 300670044329;     (3) 5.4-oz. (38 servings) bottles, UPC 300670044381;     (4) 8.6-oz. (62 servings) bottles, UPC 300670044626;     (5) 12.3-oz. (90 servings) bottles, UPC 300670044909;     (6) 16.7-oz. (125 servings) bottles, UPC 300670044831;     (7) 1.6-lb. (190 servings) bottles, UPC 300670044190;     (8) 20.2-oz .(125+25=150 servings) bottles, UPC 300670174590;     (9) 10.3-oz. (62+13=75 servings) bottles, UPC 300670175757;     (10) Bulk  .12-oz. (1 serving) stick pack, UPC 300679999996;     (11) 3.45-oz. boxes containing 28/0.12-oz. stick packs, UPC 300670030285; and    (12) 4.19-oz. boxes containing 28+6/0.12-oz. stick packs, UPC 300670030346.      Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622.  Made in France.
Worldwide Distribution - USA (nationwide) and internationally to the following countries: American Samoa   Antilles  Argentina   Australia   Austria   Bangladesh   Belgium   Bolivia   Brazil   Canada   Chile   Colombia   Egypt   El Salvador   Finland   France   Germany   Great Britain   Greece   Guatemala   Hong Kong   India   Indonesia   Ireland   Italy   Jamaica   Japan   Korea   Lebanon   Libya   Malaysia   Mauritius  Mexico   Neal   New Zealand   Nicaragua   Norway   Pakistan  Panama   Peru   Philippines   Poland   Portugal   Puerto Rico   Romania   Russia   Saudi Arabia   Singapore   Slovenia   South Africa   Spain   Switzerland   Taiwan   Thailand   the Netherlands   Trinidad   Tunisia
Advanta VXT Vascular Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Product manufactured between April 3, 2012 and May 14, 2013 and can be identified by their expiration date; between April 2017 and May 2018.
Inner tray label may adhere to wall of outer tray which make it difficult to remove the tray onto the sterile field
Flixene IFG Vascular Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Advanta SuperSoft Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Flixene IFG  with Assisted Delivery Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Advanta SST Bifurcated Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Advanta VS Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Flixene Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Advanta SST Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Advanta SuperSoft Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Advanta VXT Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Flixene Trumpet Grafts >or= 6mm Flixene GW and GWT Grafts >or= 6mm  Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Advanta VS Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Worldwide Distribution - USA Nationwide in the states of  NJ, NC, TX, FL and in the countries of Austria, Belgium, Egypt, Germany, Greece, Ireland, Israel, Italy, Luxemborg, Portugal, Russia, Saudi Arabia, Slovenia, Spain, Sweden, Switzerland, Turkey, and UK.
MedStream Programmable Pump; 20ml - 91-4200US   Product Usage:  The Medstream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market. Refill Kits- are intended for use in the filling and re-filling of the Medstream pump reservoir.
Drug flow rates exceeding programmed flow rates.
MedStream Programmable Pump; 40ml - 91-4201US   Usage:  The Medstream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market. Refill Kits- are intended for use in the filling and re-filling of the Medstream pump reservoir.
Lot/Serial Number US:  NMBKB6, NMBKFF, NMBKC5, NMBKCF, NMBJ3K
MedStream Refill Kit, U.S: 91-4287   Product Usage:  The Medstream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market. Refill Kits- are intended for use in the filling and re-filling of the Medstream pump reservoir.
MedStream Refill Kit (1 unit), EMEA: 91-4289   Product Usage:  The Medstream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market. Refill Kits- are intended for use in the filling and re-filling of the Medstream pump reservoir.
MedStream Refill Kit (6 units), EMEA: 91-4290   Product Usage:  The Medstream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market. Refill Kits- are intended for use in the filling and re-filling of the Medstream pump reservoir.
MedStream Refill Kit, U.S (6 units): 91-4288   Product Usage:  The Medstream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market. Refill Kits- are intended for use in the filling and re-filling of the Medstream pump reservoir.
0 - product used for internal training purposes only
MedStream Programmable Pump; 40ml Pump EMEA 91-4201   Product Usage:  The Medstream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market. Refill Kits- are intended for use in the filling and re-filling of the Medstream pump reservoir.
MedStream Programmable Pump; 20ml Pump EMEA 91-4200   Product Usage:  The Medstream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market. Refill Kits- are intended for use in the filling and re-filling of the Medstream pump reservoir.
Apomorphine HCL  3 MG/ML INJECTABLE  Sterile  Rx Only
Lack of sterility assurance of sterile injectables.
Buprenorphine  .3 MG/ML INJECTABLE Buprenorphine  .5 MG/ML INJECTABLE  Sterile  Rx Only
Cyclosporine (A) 2% (PF) Aqueous Susp Sterile  Rx Only
Diazepam 5MG/ML INJECTABLE Sterile  Rx Only
Meloxicam  10 MG/ML INJECTABLE Sterile  Rx Only
Tacrolimus Solution 0.02% OPTHALMIC Sterile   Rx Only
Acetaminophen Tablets, 500 mg, 100-count bottles, Distributed by: Marlex Pharmaceuticals, Inc., New Castle, DE  19720, List No. 152, NDC 10135-152-01, UPC 3 10135 15201 8.
CGMP Deviations: The recalled acetaminophen tablet lot was not manufactured under current good manufacturing practices as noted by a recent inspection of the manufacturing firm.
Worldwide Distribution - USA Nationwide in the states of AZ, CA, FL, ID, LA, MA, MD, MI, MN, MO, NC, NH, NY, OH, OK, PA, SC, TX, VA, WI, and WV and the countries of: Austria, Belgium, Czech Republic, France, Germany, Greece,Hungary, Israel, Italy, Latvia, Netherlands, Poland, Portugal, Russian Federation, Slovenia, Spain, Sweden, Switzerland, United Arab, and United Kingdom
Cordis ADROIT 6F Guiding Catheter   Product Usage:  For intravascular introduction of interventional and/or diagnostic devices into the coronary or peripheral vascular system.
Due to a labeling error related to the conversion of the inner diameter of the catheter from inches to millimeters.  The English dimension is correct and is the primary dimension.
Nationwide Distribution, including the states of: AK, AL, AR, AZ, BM, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and WV.
Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The intended use is in vitro testing of samples of whole blood.
RADIOMETER became aware that some membranes may have enzyme residue on the outer membrane. The enzyme residue may cause an initial negative bias on the reported Lactate result upon replacement of the Lactate membrane.
H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01, NSN 6515-01-573-0692), vacuum sealed and packaged in a 5 mil poly bags, labeled in part ***H & H Associates, Inc. CAGE 1NNH6 www.gohandh.com Ordinary, VA 23131 (800) 326-5708***.     The product is used to maintain fracture alignment.
Lots\EXP Dates:   CKBD033, CKBE033 August 2015  CKBD034, CKBF034, CKBG034 August 2015  CKBP045 November 2015  CKBP047, CKBQ047 November 2015  CKBR060 February 2016  CKBT065 April 2016  CKBV070, CKBW070, CKBX070 May 2016  CKBX071 May 2016  CKBX076 June 2016  CKBX078 July 2016  CKBX079, CKBY079 July 2016  CKBY080, CKBZ080, CKCA080 July 2016.
Medical device tubing used for endotracheal airway application may become weakened and rendered ineffective.
Tullys House Blend Coffee 12-ct K-Cup packs; Product Code:  8802 (Case of 6 - 12 count retail boxes) UPC:  10099555088028
4,697 master cases (6 retail boxes per case)
Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.
Tully's House Blend Decaffeinated K-Cup Packs (12-ct retail box) Product Code:  8803; UPC: 099555088038
Best By:  27 MAR 2014, 28 MAR 2014 Lot Numbers:  NA PL055 3181, NA PL055 3182
Universal Flex2 Breathing Circuit Class I   510(k) Exempt    An anesthesia breathing circuit is a device that is intended to administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Y-piece.
King Systems received a customer complaint indicating that the customer had ordered a breathing circuit with a Latex breathing bag.  The product they received contained a Latex breathing bag, but was labeled as non-latex.
USA Nationwide Distribution in the state of NY
King LTS-D Oropharyngeal Airways     Product Usage:  The King LTS-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.
Part Number(s): KLTSD415 Lot Number(s): IV1V3
On December 13, 2012, King Systems initiated a voluntary recall of one (1) case(s) (5) individual products) from one (1) lot [(IV1V3) 62 cases, 310 products]of King LTSD Oropharyngeal Airways because the package label indicated that the airway was a size 5 when in fact the airway in the package was a size 4. When King manufacturers a lot, all of the components are the same size, part number etc. In this instance, the lot number IV1V3 was for size 5 King LTSD airways, part number KLTSD415. The manufacturing and inventory records show that one case (5 products) of KLTSD size 4 airways were erroneously manufactured as part of lot IV1V3. King Systems has not received any further complaints.
Worldwide Distribution -  USA including the states of AL, AR, CA, CO, FL, IL, KY, LA, NE, NC, NJ, NY, OH, PA, TN, TX, UT, WA and WV., and the countries of  Canada, Denmark, Iran, Italy, Mexico and Taiwan.
Selenia Full Field Digital Mammography System with software versions 5.0.x and 5.1.x   The Selenia Full Field Digital Mammography system generates digital mammography images that can be used for screening and diagnosis of breast cancer. The Selenia Full Field Digital Mammography System is intended for use in the same clinical applications as traditional screen-film mammography systems. Mammography images can be interpreted on either hard copy film or soft copy review workstations, cleared for mammography
Software: When the Selenia upon meeting the hard drive threshold of 4,000 images, may delete the most recently dated images
5% Lidocaine HCl and 7.5% Dextrose Injection, USP, 2 mL Single Dose Ampuls, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4712-01
Presence of Particulate Matter; report of glass particles in the ampule after dilution
Worldwide distribution: US (nationwide) including Puerto Rico and countries of: Albania, American Samoa,  Argentina, Australia, Austria, Bahrain, Barbados, Bangladesh, Belgium, Bermuda, Belize, Bolivia, Bosnia and Herzegovina, Brazil, Canada, Chile,China, Colombia, Costa Rica, Croatia, Cyprus, Czech Rep, Dominican Republic, Ecuador, Egypt, Estonia, El Salvador, Finland, France, Germany, Georgia, Greece, Guatemala, Hong Kong, Honduras, Hungary, India, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Korea, Kuwait, Latvia, Lebanon, Lithuania, Lybia Jamahiriya, Malaysia, Mexico, Moldova, Morocco, Netherlands, Nepal, Nicaragua, Norway, Oman, Pakistan, Palastine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russian Federation, Rwanda, Saudi Arabia, Singapore, Slovenia, Slovakia, Spain, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Arab Emirates, and United Kingdom.
Product Name: AVEA Ventilator. All Models.   The affected devices are cleared under K073069 pm 1/25/2008 and K103211 on 05/06/2011. This device is a Class II medical Device.    A continuous ventilator (respirator) is a device intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in the breathing gas. Adult, pediatric, and neonatal ventilators are included in this generic type of device.
CareFusion has identified a potential risk associated with AVEA ventilators when used at higher altitudes. A proactive complaint review identified an error in the barometric pressure compensation. CareFusion is voluntarily initiating a field correction of the affected devices to correct the error.
Venlafaxine (Venlafaxine Hydrochloride) extended release Tablets, 225 mg, packaged in a) 30- count bottle (NDC 0131-3268-32) and b) 90-count bottle (NDC: 0131-3268-46), Rx only, Manufactured by: Kremers Urban Pharmaceuticals Inc. For: Osmotica Pharmaceutical Corp., Wilmington, NC 28405, USA.
Failed Dissolution Specification; 12 hour time point at 18 months shelf life
Estradiol 1.25 mg, Progesterone 25 mg/mL injectable, 20 mL sterile vials, The Apothecary Shoppe, 6136 E. 51st St. Tulsa, OK 74135.
Lack of Assurance of Sterility: concerns of sterility assurance with the  pharmacy's independent testing laboratory.
SIH-Testosterone Cypionate 200 mg/mL Injectable, 10 mL sterile vial, The Apothecary Shoppe, 6136 E. 51st St. Tulsa, OK 74135.
Worldwide Distribution USA including DC, all states except HI, ND,  RI and WY and Internationally to Australia, Bahrain, Belarus, Belgium, Brazil, Canada, Chile, China, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, India, Indonesia, Israel, Italy, Japan, Korea (Republic of), Kuwait, Lebanon, Martinique, Mexico, Netherlands, New Zealand, Norway, Oman, Poland, Qatar, Russia, Saudi Arabia, Serbia, Singapore, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkey, United Arab Emirates, United Kingdom, Uruguay,    .    OUS: AUSTRALIA, AUSTRIA, BAHRAIN, BELARUS, BELGIUM, BRAZIL, CANADA, CHILE, CHINA, CROATIA, CZECH REPUBLIC, DENMARK, EGYPT, FINLAND, FRANCE, GERMANY, GREECE, HONG KONG, INDIA, INDONESIA, ISRAEL, ITALY, JAPAN, REPUBLIC OF KOREA, KUWAIT, LEBANON, MARTINIQUE, MEXICO, NETHERLANDS, NEW ZEALAND, NORWAY, OMAN, POLAND, QATAR, RUSSIA, SAUDI ARABIA, SERBIA, SINGAPORE, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM, URUGUAY.
GE Healthcare, Discovery MR750 3.0T, Optima MR450w 1.5T, and Discovery MR450 1.5T .   scanner designed to support high resolution, high signal-to-noise ratio, and short scan times. The GE Signa MR 750 System is indicated for use as a diagnostic imaging device to produce axial, sagittal, coronal, and oblique images, spectroscopic images, parametric maps, and/or spectra, dynamic images of the structures and organs of the entire body, including but not limited to, head, neck, TMJ, spine, breast, heart, abdomen, pelvis, joints, prostate, blood vessels, and musculoskeletal regions of the body. The images produced by the GE Signa MR 750 System reflect the spatial distribution or molecular environment of nuclei exhibiting magnetic resonance. These images when interpreted by a trained physician yield information that may assist in diagnosis. The indications for use for the 3.0T GE Signa MR750 System are similar to those for the Signa HDx Magnetic Resonance System and the Siemens MAGNETOM Verio MR System. K113490: The Optima'' MR450w is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times. It is indicated for use as a diagnostic imaging device to produce axial, sagittal, coronal, and oblique images, spectroscopic images, parametric maps, and/or spectra, dynamic images of the structures and/or functions of the entire body, including but not limited to, head, neck, TMJ, spine, breast, heart, abdomen, pelvis, joints, prostate, blood vessels, and musculoskeletal regions of the body. Depending on the region of interest being images, contrast agents may be used. The images produced by the Optima'' MR 450w reflect the spatial distribution or molecular environment of nuclei exhibiting magnetic resonance. These images and/or spectra when interpreted by a trained physician yield information that may assist in diagnosis. K083147: The Discovery MR 450 is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, a
GE Healthcare has recently become aware of a potential safety issue due to exposed yellow foam on the end bells of Discovery MR450, Discovery MR750, and Optima MR450w products.   The yellow foam strip used between the end bell covers and patient bore of certain GE MR Products may extend past the surface of the covers. The foam itself is not hazardous. However, any fluid or body substance absorbed by the extended foam may come into contact with patients and act as a fomite potentially transferring infectious agents from one patient to another.
Oxycodone and Acetaminophen Tablets, USP 10 mg/650 mg, CII, 100 Count Bottles, Rx Only, Manufactured by: Watson Laboratories, Inc. Corona, CA 92880 USA, NDC 0591-0825-01
Presence of Foreign Tablets/Capsules: 20 tablets of Oxycodone/APAP 7.5/500 mg were found in a sealed 100 count bottle of Oxycodone and Acetaminophen Tablets, USP 10/650 mg lot# 705791A.
Sodium Phosphate Injectable, 150mM/50mL Phosphorus 200mEq/50mL Sodium, 50 mL Single Dose Vial, Rx only, Triangle Compounding Pharmacy,  3700 Regency Parkway, Suite 140, Cary NC 27518.
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.
Histamine, 10 ng/mL Injectable, MDV, Rx only, Triangle Compounding Pharmacy, 3700 Regency Parkway, Suite 140, Cary NC 27518.
Worldwide Distribution - United States including the territories of Guam and Puerto Rico and the countries of Canada and France.
McKesson Horizon Medical Imaging (HMI) Radiological Image Processing System, product versions 4.6.1 to 11.6.,  is a medical image and information management application intended to receive, transmit, store, retrieve, display, print and process digital medical images, digital medical video, and associated medical information from medical imaging systems.
Software malfunction may occur resulting in a certain combination of server configurations which has the potential to cause image loss.
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Ifosfamide Injection 1g/20mL, Single dose vial, Rx only, Sterile, For Intravenous Use,  Refrigerate at 2-8 degrees celcius, Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017, NDC 0069-4495-22
Temperature abuse: Certain vials of Ifosfamide IV products were not refrigerated at certain Amerisource Bergen Drug Corp distribution centers.
Ifosfamide Injection 3g/60 mL, Single dose vial, Rx only, Sterile, For Intravenous Use, Refrigerate at 2-8 degrees celcius, Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017, NDC 0069-4496-22
Worldwide Distribution - USA and the countries of  Australia, Belgium, Canada, Hong Kong, Malaysia, New Zealand, Singapore, Spain, Switzerland, Taiwan and Thailand.
NC Sprinter; Rapid Exchange Balloon Dilatation Catheter; Sterile; 2.25 mm; Model NCSP22512X.  Manufacturer: Medtronic, Inc. 710 Medtronic Parkway Minneapolis, MN 55432    The NC Sprinter Rapid Exchange Balloon Dilatation Catheter is a Percutaneous Transluminal Coronary Angioplasty (PTCA) Rapid Exchange System. The balloon at the distal end of the catheter can be inflated to a defined diameter at a specific pressure (see labelling). The proximal end of the catheter has a female luer for attachment to an inflation device. The catheter provides a lumen which enables the use of a guide wire to position the catheter. Radiopaque balloon marker(s) enable accurate placement. Shaft markers for brachial and femoral techniques are in place.
Compliance chart included in lot 207002011 of the NC Sprinter RX 2.25 x 12 mm products lists the size of the device as 2.5mm instead of the correct 2.25mm size.
Worldwide Distribution - USA and the countries of  Mexico and Canada.
DeVilbiss Vacu-Aide QSU Suction Unit (Disposable Suction Container/Filter), 800 ML DISP Container, Unassembled, 800 ML DISP Container w/6' patient tubing, and 800 ML DISP Container w/6' patient tubing, assembled.   DeVilbiss Vacu-Aide QSU Suction Unit (Disposable Suction Container/Filter) is used to remove fluids from the airway or respiratory support system and infectious materials from wounds. It is available for use by consumers by physician order.
End users of the DeVilbiss Disposable Suction Container/Filter had exposed the bacterial filter cartridge to fluid, thereby occluding the filter and rendering it unusable.
Distributed in the states of ID, WI, IN, and NE.
SHOPKO Waterproof Adhesive Pads Antibacterial.   Used for covering minor cuts, scrapes and burns.
No antibacterial bandages were packed in boxes labeled as antibacterial.
USA Nationwide Distribution in the states of: Florida, Maryland, New Jersey, New York and Texas.
Ultima OPCAB System, Sterile, Rx Only,    Product Usage:  Intended for use during performance of minimally invasive cardiac surgery through a sternotomy incision approach. The ULTIMA Access RailPlatform in combination with the Activator II Drive Mechanism is used to spread the sternum, providing access and direct visualization to the thoracic cavity. The AccessRail Platform also allows for the organization of pericardial sutures. The ULTIMA Stablizer isolates and provides local immobilization of the target vessel on the beating heart.
ULTIMA OPCAB System Part Nos. OM-2003S (LOT #25052176) and OM-2001D (LOT #25052200).
MAQUET has identified a potential issue with the ULTIMA OPCAB (part numbers OM-2003S & OM-2001D).  Labeling for the 2 blade lots had been incorrectly applied.  The standard blades from Lot #25052176 were incorrectly labeled as deep blades, and the 20 deep blades from Lot #25052200 were incorrectly labeled as standard blades.