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. 2,525 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,525 in last 12 months

Showing 83618380 of 48,376 recalls

Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Implant Kit Recalled by...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· NeuroLogica Corporation

Recalled Item: OmniTom/OmniTom Elite- X-ray computed tomography applications for anatomy...

The Issue: 1. Wheels loosening over time with use of the device could lead to the...

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

Class II — Potential Health HazardOngoing
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: 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: 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
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: 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: 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
Medical DeviceJune 5, 2023· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Troponin I ES Reagent Pack Recalled by...

The Issue: Reagent packs could potentially contain incorrect wells, which will generate...

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

Class II — Potential Health HazardOngoing