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. 1,060 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
1,060 in last 12 months

Showing 8381–8400 of 48,376 recalls

DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: SnoreStop Naso Spray Bulk Recalled by Homeocare Laboratories, Inc. Due to...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: Bebelyn Colic Drops Homeopathic Remedy Recalled by Homeocare Laboratories,...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: StellaLife VEGA Oral Care Spray Recalled by Homeocare Laboratories, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: StellaLife VEGA Oral Care Rinse Recalled by Homeocare Laboratories, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: Arnica 7 Cream Recalled by Homeocare Laboratories, Inc. Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: StellaLife VEGA Oral Care Rinse Recalled by Homeocare Laboratories, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: DoloEar Earache Drops Recalled by Homeocare Laboratories, Inc. Due to cGMP...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: StellaLife VEGA Oral Care Gel Recalled by Homeocare Laboratories, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: Kanjo Homeopathic Pain Relief Cream With Arnica Recalled by Homeocare...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: Babelyn Diarrhea Drops Homeopathic Remedy Recalled by Homeocare...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 2, 2023· Beckman Coulter Biomedical GmbH

Recalled Item: Beckman Coulter DxA Automation System Recalled by Beckman Coulter Biomedical...

The Issue: A software defect in the DxA Automation System may cause tests to be run on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2023· Covidien, LLC

Recalled Item: Covidien Cytosponge Cell Collection Device Recalled by Covidien, LLC Due to...

The Issue: Cell Collection Device may be at increased risk of the sponge detaching from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2023· Beckman Coulter Biomedical GmbH

Recalled Item: Beckman Coulter DxA Automation System Recalled by Beckman Coulter Biomedical...

The Issue: A software defect in the DxA Automation System may cause tests to be run on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing