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. 2,273 recalls have been distributed to West Virginia in the last 12 months.
Showing 43121–43140 of 48,376 recalls
Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: During stability testing an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: During stability testing an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prolia (denosumab) Injection Recalled by Amgen, Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Visible cellulose fibers were observed in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens Dimension LOCI TNI Troponin I Calibrator RC 621. The Recalled by...
The Issue: Siemens Dimension LOCI TNI Troponin I calibrator lot 3DD007 may demonstrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquarius (TM) TEMPERATURE THERAPY Recalled by DeRoyal Industries Inc Due to...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1% Lidocaine HCl Injection Recalled by Hospira, Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Oxidized stainless steel found in vial of 1%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Injection Recalled by Hospira, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Confirmed customer report of leakage of vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine (Venlafaxine Hydrochloride) extended release Tablets Recalled by...
The Issue: Failed Dissolution Specification:12 hour time point at 18 months of product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: COBAS INTEGRA 800 Analyzer with software 9864.C2 Cobas. COBAS Part Recalled...
The Issue: Roche COBAS INTEGRA 800 system, Software Version 9864.C2 does not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTAX Endoscopic Accessories. OF-B194. Made in Japan. PENTAX Upper/Lower...
The Issue: PENTAX Medical has become aware of a product issue associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences EMBOL-X Glide Protection System Recalled by Edwards...
The Issue: Edwards Lifesciences is recalling certain lots of EMBOL-X Glide Protection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR Excimer Laser System with Variable Spot Scanning Recalled by Abbott...
The Issue: This corrective action will address an identified failure of the lamp and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.