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. 2,356 recalls have been distributed to West Virginia in the last 12 months.
Showing 25981–26000 of 48,376 recalls
Recalled Item: Blue Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of Colors...
The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clay Mask Kit Recalled by Plant Devas Inc Due to FDA Office of Colors and...
The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Rose Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of Colors...
The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lemongrass Facial Polish with Oats Recalled by Plant Devas Inc Due to FDA...
The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Green Tea Clay Recalled by Plant Devas Inc Due to FDA Office of Colors and...
The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: French Rose Clay Recalled by Plant Devas Inc Due to FDA Office of Colors and...
The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Blemish Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of...
The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System)...
The Issue: Recently Integrity Implants uncovered a discrepancy in the cleaning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sternal Valve Retractors With Atrial and Aortic Rakes Recalled by Genesee...
The Issue: Failure in a retractor blade due to corrosion. In the area of the blade...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wet-Field Hemostatic Eraser Bipolar 25G Recalled by Beaver-Visitec...
The Issue: Products were packaged with incorrect labeling,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RANITIDINE Tablets Recalled by Mckesson Packaging Services Due to Failed...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Evamist (estradiol transdermal spray) Recalled by Paddock Laboratories, LLC....
The Issue: Defective Delivery System: Potential that cracks in the vial neck near the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lynparza (olaparib) capsules 50 mg Recalled by AstraZeneca Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications; elevated levels of quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: T4 Zipper Toga Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4 Zipper Toga (S/M) Recalled by Stryker Instruments Div. of Stryker...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5 Zipper Toga with Peel-Away Face Shield Recalled by Stryker Instruments...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12F MODIFIED Tesio CATHETER SET Recalled by Medical Components, Inc dba...
The Issue: There is the potential for connection failures related to the female...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REPAIR KIT Recalled by Medical Components, Inc dba MedComp Due to There is...
The Issue: There is the potential for connection failures related to the female...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.