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 90619080 of 29,425 recalls

Medical DeviceSeptember 27, 2021· O&M HALYARD INC

Recalled Item: HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES Recalled by O&M...

The Issue: All lots of the glove may discolor and lose elasticity upon aging, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2021· Philips Healthcare

Recalled Item: Philips Azurion systems with software releases 2.1(L1) and 2.1(L2) Recalled...

The Issue: 3D-RA is a reconstruction software product that can be used with the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2021· TiSport, Llc

Recalled Item: Permobil TiLite Recalled by TiSport, Llc Due to Some affected wheelchairs,...

The Issue: Some affected wheelchairs, with transit tie downs, that are used as a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2021· Philips North America Llc

Recalled Item: Philips Azurion Interventional Fluoroscopic X-Ray System Recalled by Philips...

The Issue: When the user presses or releases both the APC (accept) button and the Float...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software error, the software can produce an incorrect interpretation of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2021· Implant Direct Sybron Manufacturing LLC

Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...

The Issue: Packaged dental implant contains a different size then the size declared on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2021· Implant Direct Sybron Manufacturing LLC

Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...

The Issue: Packaged dental implant contains a different size then the size declared on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2021· Medtronic Neuromodulation

Recalled Item: Clinician Programmer Application (CPA) model A610 Clinician Software...

The Issue: A software anomaly may occur with the clinician programmer application.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2021· DiaSorin Molecular LLC

Recalled Item: SIMPLEXA COVID-19 Positive Control Pack Recalled by DiaSorin Molecular LLC...

The Issue: Due to unapproved raw materials used in the manufacturing of Covid-19...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation/RayPlan versions 4 - 11A Recalled by RAYSEARCH LABORATORIES AB...

The Issue: An issue where the combined density in a dose grid voxel partially covered...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS TOXO IgG Avidity (TXGA) Recalled by bioMerieux, Inc. Due to bioMerieux...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS SARS-COV-2 IgM Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS RUB IgG (RBG) Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS FSH Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Estradiol II Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Lyme IgG II (LYM) Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS PRG Progesterone Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Measles IgG (MSG) Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Clostridium Difficile GDH Recalled by bioMerieux, Inc. Due to...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing