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. 1,091 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
1,091 in last 12 months

Showing 1881–1900 of 48,376 recalls

Medical DeviceJuly 7, 2025· Boston Scientific Corporation

Recalled Item: Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding Stent...

The Issue: Certain batches are being removed due to an increase in complaints received...

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

Class I — Serious Health HazardOngoing
DrugJuly 7, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: H-E-B Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Subpotent Drug-...

The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 7, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: RITE AID PHARMACY Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 7, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 7, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ReliOn Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Subpotent...

The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 7, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CURAD Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 7, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Good Neighbor Pharmacy Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 5, 2025· FDC Limited

Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...

The Issue: Defective Container: spike of the cap becomes lodged in the nozzle of the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: C9-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: C8-4v Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: OMNI II TEE Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: S9-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: mC7-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: X6-1 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: S5-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: VL13-5 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: eL18-4 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: S4-1 Lumify Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: S4-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: X5-1c Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing