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. 2,318 recalls have been distributed to West Virginia in the last 12 months.
Showing 38501–38520 of 48,376 recalls
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to Labeling; The affected...
The Issue: Labeling; The affected product packaging is incorrectly labeled as being a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Select Kits (ASK) Recalled by Arrow International Inc Due to Certain...
The Issue: Certain product codes and lot numbers of Kits with Biopatch Dressing were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5-methyltetrahydrofolate Calcium (L) (a) 1 gm in 2 oz container Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CS 8100 Recalled by Carestream Health, Inc. Due to Units device head...
The Issue: Units device head descended unexpectedly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 8100 3D Recalled by Carestream Health, Inc. Due to Units device head...
The Issue: Units device head descended unexpectedly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This correction applies to all GE Healthcare MRI systems with Recalled by GE...
The Issue: At certain sites, the MRU may not be connected to the magnet. In emergency...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cold Therapy Pad - cold water circulating pad Recalled by Cincinnati...
The Issue: Seals in the water path of the CT-99 cold therapy pad may separate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 6 Aseptic Housing. The Stryker System 6 Aseptic Housings Recalled by...
The Issue: Stryker is recalling System 6 Aseptic Housing, due to a failed Continuous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benzonatate Capsules Recalled by American Health Packaging Due to Failed...
The Issue: Failed Tablet/Capsule Specifications; recall initiated by manufacturer due...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BARBECUE SP RIB RUB 50 lb. Con Yeager Spice Company Recalled by Con Yeager...
The Issue: Cumin and cumin containing spice mixes may contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Con Yeager Spice Company Recalled by Con Yeager Spice Co Due to Undeclared...
The Issue: Cumin and cumin containing spice mixes may contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.