Product Recalls in Virginia

Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,122 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,122 in last 12 months

Showing 8741–8760 of 29,425 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· 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 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 22, 2021· Empowered Diagnostics LLC

Recalled Item: CovClear COVID-19 Rapid Antigen Test Recalled by Empowered Diagnostics LLC...

The Issue: COVID test kits were offered for sale and distributed to consumers in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2021· Empowered Diagnostics LLC

Recalled Item: ImmunoPass Recalled by Empowered Diagnostics LLC Due to COVID test kits were...

The Issue: COVID test kits were offered for sale and distributed to consumers in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Repair Kit Recalled by Philips Respironics, Inc. Due to Philips...

The Issue: Philips has identified a specific lot of non-conforming material...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Philips has...

The Issue: Philips has identified a specific lot of non-conforming material...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: DREAMTOME 49-30MM/450CM Material Number: M00584030 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· Medtronic Xomed, Inc.

Recalled Item: NIM TRIVANTAGE EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due...

The Issue: There is potential for multiple issues due to a manufacturing nonconformity.

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

Class II — Potential Health HazardOngoing