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. 2,821 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,821 in last 12 months

Showing 57215740 of 29,425 recalls

Medical DeviceAugust 31, 2023· Pulmonx, Corp.

Recalled Item: Zephyr Endobronchial Valve (EBV) 5.5-LP Recalled by Pulmonx, Corp. Due to...

The Issue: Endobronchial implant devices may have been labeled with a shortened...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Access Vascular, Inc

Recalled Item: HydroPICC 5Fr Dual Lumen Recalled by Access Vascular, Inc Due to Specific...

The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Access Vascular, Inc

Recalled Item: HydroPICC 5Fr Dual Lumen Maximal Barrier Kit Recalled by Access Vascular,...

The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Philips North America Llc

Recalled Item: EarlyVue VS30 Vitals Monitor Recalled by Philips North America Llc Due to A...

The Issue: A software issue prevents the monitor from alarming when the high/low...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Philips North America Llc

Recalled Item: EarlyVue VS30 Vital Signs Monitor Recalled by Philips North America Llc Due...

The Issue: A software issue prevents the monitor from alarming when the high/low...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: Citrine Triple Quad Mass Spectrometer Recalled by AB Sciex, LLC Due to In...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: 4500MD Triple Quad Mass Spectrometer Recalled by AB Sciex, LLC Due to In...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing