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. 2,716 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,716 in last 12 months

Showing 53615380 of 29,286 recalls

Medical DeviceNovember 2, 2023· Biomet, Inc.

Recalled Item: Biolox Ceramic Option Head Zimmer 12/14 40mm +0 Recalled by Biomet, Inc. Due...

The Issue: One product complaint was received reporting that there was an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2023· Biomet, Inc.

Recalled Item: Biolox Ceramic Option Head Zimmer 12/14 40mm -3 Recalled by Biomet, Inc. Due...

The Issue: One product complaint was received reporting that there was an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· Turncare, Inc

Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...

The Issue: A software issue where "low" and "terminal" battery alerts did not display...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· Atrium Medical Corporation

Recalled Item: Atrium Oasis Drain Single W / AC Recalled by Atrium Medical Corporation Due...

The Issue: A sterilization nonconformance prematurely aged the product by 48.3 days,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· Stryker Spine

Recalled Item: LITe Decompression Snake Arm Recalled by Stryker Spine Due to Product arm...

The Issue: Product arm was manufactured with the incorrect clamp component. As a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Change Healthcare Stratus Imaging PACS 1.4 and Stratus Imaging Share 1.4...

The Issue: Under certain circumstances, information from HL7 messages received by...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· B. Braun Medical, Inc.

Recalled Item: Infusomat Administration Sets as listed below: 362031 Infusomat Space Pump...

The Issue: In affected products, the tubing outer diameter may vary in size or the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ADLT BLOOD CULTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: PERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: 24 BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTRAL LINE BLOOD CULTURE DRA Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2023· Zeus Scientific, Inc.

Recalled Item: ZEUS ELISA Parvovirus B19 IgM Test System Recalled by Zeus Scientific, Inc....

The Issue: The organization completed a product improvement process to the conjugate...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2023· Zeus Scientific, Inc.

Recalled Item: ZEUS ELISA Parvovirus B19 IgG Test System Recalled by Zeus Scientific, Inc....

The Issue: The organization completed a product improvement process to the conjugate...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2023· Maquet Cardiovascular, LLC

Recalled Item: Acrobat-i Vacuum Positioner System Recalled by Maquet Cardiovascular, LLC...

The Issue: The Positioner Arm may not tighten or lock during normal use.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2023· BioReference Health, LLC

Recalled Item: The 4Kscore Test Recalled by BioReference Health, LLC Due to Mathematical...

The Issue: Mathematical modeling of the 4Kscore with and without DRE information was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2023· Folsom Metal Products, Inc.

Recalled Item: Small DKS Disposable Kerrison System Recalled by Folsom Metal Products, Inc....

The Issue: Units were not intended for commercial distribution and inadvertently...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2023· Folsom Metal Products, Inc.

Recalled Item: DKS Disposable Kerrison System Recalled by Folsom Metal Products, Inc. Due...

The Issue: Units were not intended for commercial distribution and inadvertently...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2023· KENT IMAGING, INC.

Recalled Item: Snapshot NIR Recalled by KENT IMAGING, INC. Due to Tissue oxygenation...

The Issue: Tissue oxygenation measurement system touchscreens may be unresponsive,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 250-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

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

Class II — Potential Health HazardOngoing