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. 2,367 recalls have been distributed to West Virginia in the last 12 months.
Showing 24861–24880 of 27,884 recalls
Recalled Item: ITST ANTI-ROTATION SCREW and FEM IM NAIL (10MM Recalled by Zimmer, Inc. Due...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HERBERT MINI BONE SCREW 2 and HERBERT/WHIPPLE C ANN BONE. Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEM HD ION (various sizes) Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Item codes starting with 001930 LAG SCR 12.7D X 55MM SHOR up to 155 MM...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MODULAR AUSTIN MOORE FENE. Item codes starting with 45502001 Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOORE HIP PROS LONG FENES Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System: One 1 g...
The Issue: Incorrect instructions for use (IFU).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System Recalled by...
The Issue: Incorrect instructions for use (IFU).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HGE Healthcare Patient Monitor B30 Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E9 ultrasound system. GE Vivid E9 is a Recalled by GE Healthcare,...
The Issue: GE became aware of a potential safety issue due to a system slow down and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Computed Tomography X-Ray System Recalled by Philips Medical...
The Issue: If the couch, with the footrest extension attached, is positioned where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safire Duo Ablation Catheter MediGuide Enabled Recalled by St. Jude Medical...
The Issue: St. Jude Medical Cardiovascular and Ablation Technologies Division is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Mixing Cup Arrays utilized on VITROS 250 Recalled...
The Issue: Ortho Clinical Diagnostics issued a product correction notification for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...
The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...
The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova StatStrip/StatSensor Hospital Blood Glucose Meter Recalled by Nova...
The Issue: Revised Battery Instructions for Removal and Expiration Date due to battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juggerknotless Drill Bit Recalled by Biomet, Inc. Due to Investigation...
The Issue: Investigation identified that the design of the drill bit may make the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariAx Compression Plating System Recalled by Stryker Howmedica Osteonics...
The Issue: Stryker received two reports indicating that during screw insertion under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Optima CT520 and Optima CT540 Computed Tomography (CT) systems. Recalled...
The Issue: There is an issue with the Manual Film Composer feature on some CT products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.