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. 2,563 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,563 in last 12 months

Showing 13411360 of 48,376 recalls

Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock Universal Vented Vial Spike Recalled by ICU Medical,...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2025· Iantrek Inc.

Recalled Item: Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300....

The Issue: Potential for compromised integrity of the sterile packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2025· Iantrek Inc.

Recalled Item: C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120....

The Issue: Potential for compromised integrity of the sterile packaging.

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

Class II — Potential Health HazardOngoing
DrugSeptember 5, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 5mg Recalled by Endo USA, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 5, 2025· Apotex Corp.

Recalled Item: Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution Recalled by Apotex...

The Issue: Lack of Assurance of Sterility; atypical weight loss due to improper bottle...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 5, 2025· Apotex Corp.

Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Apotex Corp. Due to...

The Issue: Lack of Assurance of Sterility; atypical weight loss due to improper bottle...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 5, 2025· Sandoz Inc

Recalled Item: Cyclophosphamide Injection 500 mg/5 mL (100 mg/mL) Recalled by Sandoz Inc...

The Issue: cGMP deviations: Temperature excursion during transportation.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 5, 2025· Spacelabs Healthcare, Inc.

Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...

The Issue: Due to display cables used for monitors were not in compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2025· Spacelabs Healthcare, Inc.

Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...

The Issue: Due to display cables used for monitors were not in compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2025· Spacelabs Healthcare, Inc.

Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...

The Issue: Due to display cables used for monitors were not in compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2025· MICROVENTION INC.

Recalled Item: Flow Re-Direction Endoluminal Devices: FRED 27 Recalled by MICROVENTION INC....

The Issue: Flow diverter may have a manufacturing issue related to the tantalum length...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2025· GE Medical Systems, SCS

Recalled Item: AW Server 2.0 Recalled by GE Medical Systems, SCS Due to Firm has identified...

The Issue: Firm has identified a security vulnerability in AW Server products. If...

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

Class II — Potential Health HazardOngoing
FoodSeptember 4, 2025· ONE FROZEN, LLC

Recalled Item: Good and Gather brand Southwest-Style Burrito Bowl Blend Processed in...

The Issue: Product may contain undeclared shrimp (crustacean shellfish).

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Entecavir Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed...

The Issue: Failed Impurity/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Entecavir Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed...

The Issue: Failed Impurity/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description HSAN63N ANGIO PACK IHAN02W...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description BFCT04X CATARACT PACK -...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description BUCY78E CYSTO PACK CMCP10X...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item number/ Product description AHLD15X LABOR...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits IHDC30R D AND C PACK Recalled by American Contract...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing