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. 2,393 recalls have been distributed to West Virginia in the last 12 months.
Showing 20541–20560 of 48,376 recalls
Recalled Item: Esthetic Abutment CC RP 1.5 mm pre-manufactured prosthetic components...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temporary Abutment Engaging CC RP pre-manufactured prosthetic components...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus XR/a (SlOK : K993090) Recalled by GE Healthcare, LLC Due to...
The Issue: Intermittently not receiving an audible exposure indication upon completion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline SYRINGE Recalled by Medline Industries Inc Due to Samples in the...
The Issue: Samples in the identified lot were found to have incomplete or open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Snappy Abutment 5.5 CC RP 3 mm Recalled by Nobel Biocare Usa Llc Due to...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Base CC RP 1.5 mm Recalled by Nobel Biocare Usa Llc Due to...
The Issue: Packages of abutments (universal base) may contain an incorrect screw. While...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temporary Snap Abutment Engaging CC RP 1.5 mm Recalled by Nobel Biocare Usa...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temporary Abutment Non-Engaging CC RP pre-manufactured prosthetic components...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Nexframe Stereotactic System and StealthStation Cranial software...
The Issue: Entry point and lead placement inaccuracies during deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rheumatoid Factor Standard (RF CAL) Catalogue Number: RF2301 GTIN:...
The Issue: The assigned value for Rheumatoid Factor over recovers against the material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Protein Calibrators (SP CAL (LIQ)) Catalogue Number: IT2691 GTIN:...
The Issue: The assigned value for Rheumatoid Factor over recovers against the material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Liquid Gel...
The Issue: Microbial Contamination of Non-Sterile Products: products were found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Soothing Sore Relief (lidocaine) Liquid Gel Recalled by Ridge Properties,...
The Issue: Superpotent Drug: products were found to be contaminated and above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Cream Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products: products were found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbamazepine Recalled by American Health Packaging Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Soothing Sore Relief (lidocaine) Cream Recalled by Ridge Properties, LLC Due...
The Issue: Superpotent Drug: products were found to be contaminated and above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Superior Pain & Itch Relief (lidocaine) Cream Recalled by Ridge Properties,...
The Issue: Superpotent Drug: products were found to be contaminated and above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Superior Pain & Itch Relief (lidocaine) Liquid Gel Recalled by Ridge...
The Issue: Superpotent Drug: products were found to be contaminated and above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vivitrol (naltrexone for extended-release injectable suspension) 380...
The Issue: Labeling: Not Elsewhere Classified. Drug product kit recalled due to 1 inch...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AQURE basic sytem Recalled by Radiometer Medical ApS Due to The firm has...
The Issue: The firm has become aware that there is a potential problem relating to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.