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. 2,404 recalls have been distributed to West Virginia in the last 12 months.
Showing 20261–20280 of 27,884 recalls
Recalled Item: 10mm X 12o Solitaire Ti Medium Spacer Solitaire Anterior Spinal System...
The Issue: Zimmer Biomet Spine initiated a recall of certain Solitaire Ti Spacers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration with Tomosynthesis functionality Recalled by Siemens...
The Issue: A potential system fatal error may occur during tomosynthesis reconstruction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Clamp¿ System (IFU : SNA027-N-90001). Provides the stability...
The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Inform II Base Unit as a part of the Recalled by Roche Diagnostics...
The Issue: Accu-Chek Inform II Base Unit might produce physical transmission errors in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eValueMed Infant Transport Mattress 301-1015 Recalled by Philips Electronics...
The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraFlex IAB: 7.5Fr 40cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Group A Strep Direct (MOL2850) with Direct Amplification Disc...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: evaluemed Infant Heel Warmer 301-1223 Recalled by Philips Electronics North...
The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra 8 IAB: 8Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RediGuard IAB: 7Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraFlex IAB: 7.5Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is Recalled by Arrow...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc.,...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Denali Filter-Femoral Delivery System Product Code: DL900F/DL950F Recalled...
The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...
The Issue: A report can be confirmed with the incorrect patient demographics resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.