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. 2,807 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,807 in last 12 months

Showing 72217240 of 29,425 recalls

Medical DeviceNovember 29, 2022· Acumed LLC

Recalled Item: Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose...

The Issue: Distribution without Pre-Market Clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2022· Universal Meditech Inc.

Recalled Item: Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid...

The Issue: Distribution of SARS-CoV-2 Antigen Rapid Test Kits without FDA market...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 28, 2022· DeRoyal Industries Inc

Recalled Item: DeRoyal Tonsillectomy Tray Recalled by DeRoyal Industries Inc Due to DeRoyal...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2022· Emergent Protective Products USA Inc

Recalled Item: RSDL (Reactive Skin Decontamination Lotion) Kit Recalled by Emergent...

The Issue: Complaints of leaking packets were received.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos Agile Max (VE10 Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos dRF Max (VE10 Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: LUMINOS Lotus Max (VF11) Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 300 dialyzers. Indicated for treatment of chronic and acute...

The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...

The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 Dialyzer. Product Code: 114749M. Not distributed in the...

The Issue: Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 Dialyzer. Product Code: 114746L. Used to treat chronic...

The Issue: Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...

The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Randox Laboratories Ltd.

Recalled Item: Liquid Assayed Specific Protein Control Level 2- In vitro diagnostic use...

The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Randox Laboratories Ltd.

Recalled Item: Liquid Assayed Specific Protein- In vitro diagnostic use Recalled by Randox...

The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Randox Laboratories Ltd.

Recalled Item: Liquid Assayed Specific Protein Control Level 3- In vitro diagnostic use...

The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips SmartPath to Ingenia Elition X MR System Recalled by Philips North...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips MR 7700 System Recalled by Philips North America Llc Due to Gradient...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips Ingenia Elition S MR System Recalled by Philips North America Llc...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips Ingenia Elition X MR System Recalled by Philips North America Llc...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips Upgrade to MR 7700 System Recalled by Philips North America Llc Due...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing