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. 2,563 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,563 in last 12 months

Showing 15211540 of 27,884 recalls

Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

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

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips X8-2t Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips V6-2 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips S5-1 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips S7-2 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips 3D9-3v Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips X7-2t Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips X5-1 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips S8-3t Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips XL14-3 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips C5-1 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips L12-4 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

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

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips L8-4 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips L9-3 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips S7-3t Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Encore Medical, LP

Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...

The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Encore Medical, LP

Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...

The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe...

The Issue: Due to an error in assembly of the thermistor within some units, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Encore Medical, LP

Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...

The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...

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

Class II — Potential Health HazardOngoing