Product Recalls in West Virginia

Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,393 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,393 in last 12 months

Showing 2126121280 of 27,884 recalls

Medical DeviceSeptember 10, 2015· Biosense Webster, Inc.

Recalled Item: Carto 3 EP Navigation System. Electro physiology system which views Recalled...

The Issue: Image disappeared from the cardiac ultrasound system when the CARTO 3 EP...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Smith & Nephew, Inc., Endoscopy Div.

Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm Recalled...

The Issue: Sterility of device is compromised due to breach in the packaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Smith & Nephew, Inc., Endoscopy Div.

Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 6.5 mm Recalled...

The Issue: Sterility of device is compromised due to breach in the packaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Smith & Nephew, Inc., Endoscopy Div.

Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 8.5 mm Recalled...

The Issue: Sterility of device is compromised due to breach in the packaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2015· Abbott Laboratories, Inc

Recalled Item: ARCHITECT i2000SR System The Abbott ARCHITECT System is intended for...

The Issue: Incorrect tubing.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2015· Intuitive Surgical, Inc.

Recalled Item: Fluorescence Imaging Procedure Kits used with the da Vinci Si Recalled by...

The Issue: B. Braun 2 gang 4-way stopcocks in the Fluorescence Imaging Procedure Kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Prism Medical C-300 Consumer Ceiling Lift Recalled by ErgoSafe Products, LLC...

The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis...

The Issue: Complaints that the femoral head could not be assembled with its...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Prism Medical P-300 Portable Consumer Lift Recalled by ErgoSafe Products,...

The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· DePuy Orthopaedics, Inc.

Recalled Item: Specialist 2 Intramedullary (SP2 IM) Rod 400mm Instrument (PN 96-6120)...

The Issue: DePuy Orthopaedics, Inc. is initiating a voluntary recall of select lots of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· Stryker Spine

Recalled Item: Stryker UniVise Spinous Process Fixation Plate System Inserter Recalled by...

The Issue: The Inserter Inner Shaft would not fit through the Inserter. The inner...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2015· Dako North America Inc.

Recalled Item: EnVision FLEX/HRP visualization reagent found in the following kits:...

The Issue: There is a defect in one lot of a buffer, non-specific background staining...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2015· Synthes (USA) Products LLC

Recalled Item: 5.0mm Unit Rod 270mm Recalled by Synthes (USA) Products LLC Due to This...

The Issue: This product was produced using a finishing process not identified as part...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2015· Steris Corporation

Recalled Item: AMSCO 400 and AMSCO C Small Steam Sterilizers Recalled by Steris Corporation...

The Issue: In AMSCO Small Steam Sterilizers equipped with the CS-iQ feature, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 3, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas b 123 POC system The cobas b 123 POC Recalled by Roche Diagnostics...

The Issue: under specific settings, an issue may occur during simultaneous Sensor...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2015· Zimmer Gmbh

Recalled Item: Zimmer Natural Nail CM Long. Intramedullary Fixation Rod. The Zimmer...

The Issue: In about 5% of tested samples, the outer tray was found to be compromised....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2015· Synthes (USA) Products LLC

Recalled Item: Inserter for Titanium Elastic Nails (TEN) Recalled by Synthes (USA) Products...

The Issue: potential for mechanical failures such as breakage.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2015· Bausch & Lomb Inc Irb

Recalled Item: BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A) Recalled by Bausch & Lomb...

The Issue: The firm determined that 25 lots had been manufactured with a minor surface...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2015· Leica Microsystems, Inc.

Recalled Item: Novocastra Lyophilized Mouse Monoclonal Antibody CD10 (CD10)....

The Issue: These Lot numbers are not stable up to the expiry date on the product labeling.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic CryoConsole Recalled by Medtronic Inc. Cardiac Rhythm Disease...

The Issue: An issue with a USB memory component contained within a subset of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing