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 2934129360 of 48,376 recalls

DrugApril 19, 2017· Qualgen

Recalled Item: Estradiol 20 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...

The Issue: CGMP deviations- Lack of Quality Assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2017· Qualgen

Recalled Item: Estradiol 18 mg pellet Recalled by Qualgen Due to CGMP deviations- Lack of...

The Issue: CGMP deviations- Lack of Quality Assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2017· Gentell, Inc

Recalled Item: Shield and Protect Moisture Barrier Cream Recalled by Gentell, Inc Due to...

The Issue: GMP Deviations; product may not meet cGMP requirements

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2017· Qualgen

Recalled Item: Estradiol 25 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...

The Issue: CGMP deviations- Lack of Quality Assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2017· Qualgen

Recalled Item: Estradiol 6 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...

The Issue: CGMP deviations- Lack of Quality Assurance

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 19, 2017· Olympus Corporation of the Americas

Recalled Item: High Frequency Resection Electrodes Recalled by Olympus Corporation of the...

The Issue: Loop wires breaking at the distal end of the Monopolar HF Resection Electrodes.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2017· Abbott Laboratories

Recalled Item: ARCHITECT SHBG Reagent The ARCHITECT SHBG assay is a chemiluminescent...

The Issue: Firm has identified that ARCHITECT SHBG results generated with the Potassium...

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

Class II — Potential Health HazardOngoing
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: CO-Q-10 OIL 20ML MDV (CALIF) 25MG/ML INJ Recalled by Key Pharmacy and...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: ZRECT for Women Herbal Dietary Supplement Capsules Recalled by Organic...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: Cummor Natural Male Enhancement Recalled by Organic Herbal Supply Due to...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: TORNADO Male Enhancement Herbal Dietary Supplement Capsules Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: ZRECT Male Enhancement Herbal Dietary Supplement Capsules Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: UPROAR All Natural Male Enhancement Herbal Dietary Supplement Capsules...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: LabidaMAX Herbal Dietary Supplement Capsules Recalled by Organic Herbal...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: RECTALIS Male Enhancement Herbal Dietary Supplement Capsules Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: HYDROXO-B12 INH PF GV 5MG/ML SOLN Recalled by Key Pharmacy and Compounding...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: 5-MTHF 10ML SDV (CALIF) 5MG/ML INJ Recalled by Key Pharmacy and Compounding...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: PROCAINE HCL 50ML MDV (CALIF) 1% INJ Recalled by Key Pharmacy and...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: TRI MIX 10/30/1 5ML MDV MCG/MG/MG/ML INJ Recalled by Key Pharmacy and...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: TRI MIX 10/15/2.5 5ML MDV MCG/MG/MG/ML INJ Recalled by Key Pharmacy and...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund