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. 2,356 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,356 in last 12 months

Showing 2574125760 of 48,376 recalls

FoodMarch 30, 2018· Nutrizone LLC

Recalled Item: Pain Out Thai Kratom all packages Recalled by Nutrizone LLC Due to Potential...

The Issue: Dietary supplements have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 30, 2018· Nutrizone LLC

Recalled Item: Cali Thai Kratom all packages Recalled by Nutrizone LLC Due to Potential...

The Issue: Dietary supplements have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 29, 2018· purely elizabeth.

Recalled Item: Chocolate Sea Salt Probiotic Granola Recalled by purely elizabeth. Due to...

The Issue: Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 29, 2018· Stryker Sustainability Solutions

Recalled Item: Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP)...

The Issue: Thrombogenicity test results demonstrated that both the test devices (SSS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2018· GE Medical Systems, SCS

Recalled Item: Discovery IGS 730 Interventional Fluoroscopic X-ray Systems Recalled by GE...

The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2018· GE Medical Systems, SCS

Recalled Item: Discovery IGS 740 Interventional Fluoroscopic X-ray Systems Recalled by GE...

The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2018· GE Medical Systems, SCS

Recalled Item: Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems...

The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...

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

Class II — Potential Health HazardOngoing
DrugMarch 29, 2018· United Pacific Co Ltd

Recalled Item: Zhong Hua Jiu (menthol 1%) Patch Recalled by United Pacific Co Ltd Due to...

The Issue: CGMP Deviations: the product was produced with substandard GMP manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2018· Akorn, Inc.

Recalled Item: 24-HOUR Oral Care q2 Kit with Ballard* Technology Recalled by Akorn, Inc....

The Issue: Subpotent Drug: Product crystallization with accompanying low out of...

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

Class III — Low RiskOngoing
Refund
DrugMarch 29, 2018· Akorn, Inc.

Recalled Item: Chlorhexidine Gluconate Oral Rinse Recalled by Akorn, Inc. Due to Subpotent...

The Issue: Subpotent Drug: Product crystallization with accompanying low out of...

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

Class III — Low RiskOngoing
Refund
DrugMarch 29, 2018· Akorn, Inc.

Recalled Item: 24-HOUR Oral Care q4 Kit with Ballard* Technology Recalled by Akorn, Inc....

The Issue: Subpotent Drug: Product crystallization with accompanying low out of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 29, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Segmental System Proximal Femoral Component 38mm Offset Recalled by...

The Issue: There is a potential for debris in the hole on the superior lateral aspect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Draegar Medical Systems, Inc.

Recalled Item: Infinity Acute Care System (lACS) Monitoring Solution Recalled by Draegar...

The Issue: Software anomaly resulting in the loss of patient settings and stored...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...

The Issue: The dose calculation accuracy may in some situations be less than expected....

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

Class II — Potential Health HazardOngoing