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. 2,521 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,521 in last 12 months

Showing 1020110220 of 48,376 recalls

DrugDecember 8, 2022· McGuff Compounding Pharmacy Services, Inc.

Recalled Item: Thiamine Hydrochloride 200 mg/2mL (100mg/mL) Recalled by McGuff Compounding...

The Issue: Presence of Particulate Matter: Presence of foreign substances were reported...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2022· McGuff Compounding Pharmacy Services, Inc.

Recalled Item: Thiamine Hydrochloride 3000 mg/30 mL (100mg/mL) Recalled by McGuff...

The Issue: Presence of Particulate Matter: Presence of foreign substances were reported...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 8, 2022· TELEFLEX LLC

Recalled Item: Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal...

The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2022· TELEFLEX LLC

Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2022· TELEFLEX LLC

Recalled Item: Endotracheal Tube labeled as the following: a. Endotracheal Tube oral/nasal...

The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2022· Medtronic Navigation, Inc.

Recalled Item: RadiaLux Lighted Retractor (Pink) Recalled by Medtronic Navigation, Inc. Due...

The Issue: Defect in sterile pouch seal, incomplete seal, of lighted Retractors,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2022· Detect Headquarters

Recalled Item: Detect Covid-19 Test Product/Model Number: 21205 Recalled by Detect...

The Issue: There is an increased chance that the tests from affected lots may give...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 7, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS L & D TRAY...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE ARM/MINOR DRAPE CSTM Recalled...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE BREAST BIOPSY KIT Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE PERF. ASSOC. CUT DOWN TRAY...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE PREP TRAY Recalled by MEDLINE...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS NEONATAL...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE CABG PACK Recalled by MEDLINE...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE PAIN TRAY Recalled by MEDLINE...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) CENTURION MEDICAL PRODUCTS CENTRAL...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) MEDLINE GENERAL UTILITY Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE LCPH LAB DRAW KIT Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing