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 38841–38860 of 48,376 recalls
Recalled Item: IS3000 Vision Side Cart (VSC) used in conjunction with the Recalled by...
The Issue: Intuitive Surgical is initiating a voluntary correction related to da Vinci...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio PT/INR Test Strips Recalled by Alere San Diego, Inc. Due to In...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INRatio 2 Monitors - 0200431 Alere INRatio 2 PT/INR Professional Recalled by...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INRatio Monitors - 0100004 Alere INRatio PT/INR System Professional -...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp Due to...
The Issue: Presence of Particulate Matter: Confirmed customer complaints received for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product failed a known...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product failed a known...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product failed a known...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops A.C. (Tetrahydrozoline HCl 0.05% Recalled by K C Pharmaceuticals...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops Advanced Relief (Dextran 70 0.1% Recalled by K C Pharmaceuticals...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops (Tetrahydrozoline HCl 0.05%) Recalled by K C Pharmaceuticals Inc...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops Industrial Strength (Polyethylene glycol 400 1% Recalled by K C...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DBX Mix Recalled by Musculoskeletal Transplant Foundation, Inc. Due to The...
The Issue: The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET Servo Humidifier 163 Recalled by Teleflex, Inc. Due to Connector...
The Issue: Connector mount cracks which may lead to a leak failure during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensei X Robotic Catheter System Recalled by Hansen Medical Inc Due to The...
The Issue: The Set Up Joint subassembly of the Sensei X Robotic Catheter System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle- Model...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle Recalled by...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Recalled by Zimmer...
The Issue: Zimmer received a single complaint wherein a Trilogy® Fiber Metal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MitoXANTRONE Injection Recalled by Hospira Inc. Due to Failed Stability...
The Issue: Failed Stability Specifications: Product is subpotent and has out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility; improperly crimped fliptop vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.