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. 2,380 recalls have been distributed to West Virginia in the last 12 months.
Showing 23301–23320 of 27,884 recalls
Recalled Item: The Rejuvenator Chamber manufactured by Baro-Therapies Recalled by...
The Issue: The firm is distributing the Rejuvenator device without an approved 510(k).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Constrained Tibial Articular Surface...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System PS Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Constrained Posterior Stabilized Tibial...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA" The Personalized Knee System UC Tibial Articular Surface...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System CR Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTRACK250A Canaloplasty Microcatheter Kit Recalled by Ellex iScience, Inc....
The Issue: One lot may not have been properly sealed, resulting in a non-sterile device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MobileDiagnost wDR motorized portable diagnostic X-ray systems. Recalled by...
The Issue: Reports of unexpected movement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) Recalled...
The Issue: The component supplier recalled their 0.9% Sodium Chloride Injection USP BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parker Eclipse Probe Cover Recalled by Parker Laboratories, Inc. Due to...
The Issue: Parker Laboratories, Inc. received a report of an incorrect expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.