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. 2,345 recalls have been distributed to West Virginia in the last 12 months.
Showing 31861–31880 of 48,376 recalls
Recalled Item: Vanguard Distal Femoral Augment 75 X 5 RL/LM Product Usage: Recalled by...
The Issue: Contents of the package do not match the product labeling. Product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Recon Targeting Arm Guide Recalled by Zimmer Biomet, Inc. Due to Old...
The Issue: Old revisions and new revisions of the soft tissue sleeve and recon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Recon Soft Tissue Sleeve Guide Recalled by Zimmer Biomet, Inc. Due...
The Issue: Old revisions and new revisions of the soft tissue sleeve and recon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPX4 Breast Tissue Expander 650 cc : Product Usage: Tissue Recalled by...
The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artoura Breast Tissue Expander 700 cc Product Usage: Tissue expanders...
The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...
The Issue: Communication provided to emphasize that the PSA values should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MENTOR 2" Tall Height TE With Sutures 450cc PN: 354-9313 Recalled by Mentor...
The Issue: Tissue expander product mix found: CPX4 350cc was placed in a carton for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MENTOR 2" Tall Height TE With Sutures 350cc PN: 354-9312 Recalled by Mentor...
The Issue: Tissue expander product mix found: CPX4 350cc was placed in a carton for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diocto Syrup (docusate sodium) Recalled by Pharmatech LLC Due to CGMP...
The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sennazon (sennosides) Syrup Recalled by Pharmatech LLC Due to CGMP...
The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aller-Chlor (chlorpheniramine maleate) Syrup Recalled by Pharmatech LLC Due...
The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ninjacof (chlophedianol HCl and pyrilamine maleate) Liquid Recalled by...
The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Senexon Liquid (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...
The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ninjacof-A (acetaminophen Recalled by Pharmatech LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Senna Syrup (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...
The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD 23 G x .75 in. BD Vacutainer¿ Push Button Recalled by Becton Dickinson &...
The Issue: BD has received multiple reports of units associated with the 23 G x .75 in....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Permits access...
The Issue: Shipping carton labeling error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Calibrator U Recalled by Siemens Healthcare...
The Issue: Failure of analytical sensitivity with Calibrator U kit lots ending in 63...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Module Model 8110 with software version 9.15 The Recalled by...
The Issue: A software anomaly with the Alaris Syringe module software version 9.15 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Line Catheterization Kit with Sharps Safety Features Permits access...
The Issue: Shipping carton labeling error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.