Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,108 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
1,108 in last 12 months

Showing 9061–9080 of 29,286 recalls

Medical DeviceSeptember 29, 2021· Baxter Healthcare Corporation

Recalled Item: Hemodialysis Delivery System Recalled by Baxter Healthcare Corporation Due...

The Issue: If the operator initiates therapy with a saved prescription profile and...

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

Class II — Potential Health HazardOngoing
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· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM SARS-CoV-2 Antigen Assay (100 Test Kit) Recalled by Siemens...

The Issue: Data provided in the Emergency Use Authorization (EUA) submission was...

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 SARS-COV-2 IgG 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 Mumps IgG (MPG) 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· Philips Healthcare

Recalled Item: CombiDiagnost R90 is multi-functional general R/F systems. Recalled by...

The Issue: The Aleva monitor requires certain labels to be applied, some of which are...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Philips Healthcare

Recalled Item: DigitalDiagnost C90 Recalled by Philips Healthcare Due to The Aleva monitor...

The Issue: The Aleva monitor requires certain labels to be applied, some of which are...

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· Z-Medica, LLC

Recalled Item: QuikClot Combat Gauze-For Temporary External Use To Control Traumatic...

The Issue: Lack of Packaging seal integrity may result in a sterile barrier breach.

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 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