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. 1,790 recalls have been distributed to West Virginia in the last 12 months.
Showing 26141–26160 of 48,376 recalls
Recalled Item: Estradiol USP (Micronized) (Yam) for prescription compounding Recalled by...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tadalafil USP (Monohydrate) for prescription compounding Recalled by...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclobenzaprine HCl USP for prescription compounding Recalled by American...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Baclofen USP (Micronized) for prescription compounding Recalled by American...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate USP (Micronized) for prescription compounding...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcipotriene BP (Monohydrate) for prescription compounding Recalled by...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kratom capsules labeled in the following ways: 1) Divinity Kratom Recalled...
The Issue: The firm's dietary supplement products contain kratom (Mitragyna speciosa),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kratom powder labeled in the following ways 1) Enhance Your Life Recalled by...
The Issue: The firm's dietary supplement products contain kratom (Mitragyna speciosa),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Weis Sunbury Recalled by WEIS MARKETS Due to Undeclared Milk
The Issue: Penne W/Asiago Sauce and Grilled Chix Small Meal is recalled due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Stanbio AC power adapter for the HemoPoint H2 meter Recalled by Stanbio...
The Issue: The US prong (type A) adapter plate may crack, break, or detach and remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT - Model no. 728306 Computed Tomography X-Ray system Recalled...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Flex - Model no. 728317 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 6 Slice (Air) - Model no. 728256 Recalled by Philips Medical...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core - Model no. 728321 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fornier Phantom Fiber(TM) Sutures: Item Number Description SMB000425 4.5 MM...
The Issue: Data has shown that degradation of a raw material used in Phantom Fiber may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.