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 85618580 of 27,884 recalls

Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· Olympus Corporation of the Americas

Recalled Item: Spiration Valve System (SVS) Valve in Cartridge -A one-way endobronchial...

The Issue: Mislabeled Patient Charge Label indicating model number SVS-V7-00 (7mm)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: HYDRATOME RX 44-20MM/450CM Material Number: M00583060 Recalled by Boston...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: JAGTOME RX 44-20-260-035 Material Number: M00573040 Recalled by Boston...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: HYDRATOME RX 49-20MM/260CM Material Number: M00583000 Recalled by Boston...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: DREAMTOME 44-30MM/260CM Material Number: M00584050 Recalled by Boston...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: JAGTOME RX 39-30-260-025 Material Number: M00573100 Recalled by Boston...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: JAGTOME RX 39-20-450-025 Material Number: M00573090 Recalled by Boston...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: JAGTOME REVOLUTION RX 39-20-260-025 Material Number: M00584240 Recalled by...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: DREAMTOME 49-20MM/260CM Material Number: M00584000 Recalled by Boston...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing