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. 2,547 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,547 in last 12 months

Showing 36813700 of 48,376 recalls

Medical DeviceNovember 14, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES 7 Drawer Auxiliary Tower Recalled by CareFusion 303,...

The Issue: Due to a software issue, automated dispensing cabinet devices may open the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Due to a...

The Issue: Due to a software issue, automated dispensing cabinet devices may open the...

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

Class II — Potential Health HazardOngoing
DrugNovember 13, 2024· Brands International Corporation

Recalled Item: Kissable Diabetics Foot Cream Recalled by Brands International Corporation...

The Issue: CGMP Deviations: lack of adequate release testing.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 13, 2024· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: The DxI 9000 Access Immunoassay Analyzer wash wheel mixer may not spin...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2024· Alcon Research LLC

Recalled Item: Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Recalled...

The Issue: Increase in complaints associated with a molding defect within the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· Aerin Medical, Inc.

Recalled Item: Aerin Medical VivAer Stylus Recalled by Aerin Medical, Inc. Due to Some...

The Issue: Some units in a single production lot were programmed incorrectly which will...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ST REPROCESSED BRUNS CURETTE #00 (BC00) Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Magnesium Flex reagent cartridge Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics is recalling two lots of their Dimension...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ST OR MAYO HEGAR NEEDLEHOLDER 6"(OR2500) Recalled by MEDLINE INDUSTRIES, LP...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE MAGILL FORCEP (MAGF9) Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: O.R. SCISSORS Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: RUMMELL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak seals...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE STRT KELLY HEMOSTAT (SK8039S) Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ST IUD REMOVAL HOOK 10" (504090) Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
FoodNovember 11, 2024· House Of Flavors, Inc.

Recalled Item: Giant Eagle churned Butter Pecan Reduced Fat 48FLOZ Recalled by House Of...

The Issue: Undeclared soy (soy lecithin).

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2024· American Regent, Inc.

Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...

The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2024· American Regent, Inc.

Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...

The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2024· American Regent, Inc.

Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...

The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2024· Safecor Health, LLC

Recalled Item: Aspirin Chewable tablet 81 mg Recalled by Safecor Health, LLC Due to cGMP...

The Issue: cGMP Deviations: Observations were made that some blister card-foils were...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2024· Safecor Health, LLC

Recalled Item: Calcium Carbonate Chewable 500 mg Recalled by Safecor Health, LLC Due to...

The Issue: cGMP Deviations: Observations were made that some blister card-foils were...

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

Class II — Potential Health HazardOngoing
Refund