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 54615480 of 53,342 recalls

Medical DeviceJune 17, 2024· Megadyne Medical Products, Inc.

Recalled Item: Brand Name: MEGADYNE" MEGA SOFT" Reusable Patient Return Electrode Product...

The Issue: To limit the use of the Mega Soft Pads to patients aged 12 or older to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Outlook OUTLOOK PUMP SET Recalled by B. Braun Medical, Inc. Due to Potential...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV. 15 DROP PUMP SET W/ 0.2 FILTER- Used Recalled by B. Braun...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat SPACE PUMP IV SET 15D Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump Recalled by Baxter Healthcare...

The Issue: Improperly performed testing prior to release

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2024· Abbott Laboratories

Recalled Item: Alinity hq Analyzer Recalled by Abbott Laboratories Due to 1)If Complete...

The Issue: 1)If Complete Blood Count with differential and reticulocyte(CBC+Diff+Retic)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2024· B Braun Medical Inc

Recalled Item: Brand Name: Perfusor Space Product Name: Perfusor PCA Syringe Pump Recalled...

The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2024· Medical Depot Inc.

Recalled Item: Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury...

The Issue: The tiller separates from the base/front caster assembly. If the knee walker...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2024· Medical Depot Inc.

Recalled Item: Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury...

The Issue: The tiller separates from the base/front caster assembly. If the knee walker...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2024· B Braun Medical Inc

Recalled Item: Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump...

The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2024· B Braun Medical Inc

Recalled Item: Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump...

The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2024· Beckman Coulter, Inc.

Recalled Item: Discrete photometric chemistry analyzer for clinical use. Recalled by...

The Issue: Beckman Coulter, Inc. has identified a rise in reagent carousel motion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2024· B Braun Medical Inc

Recalled Item: Brand Name: Perfusor Space Product Name: Perfusor Space Infusion Pump...

The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2024· B Braun Medical Inc

Recalled Item: Brand Name: Perfusor Space Product Name: PERFUSOR SPACE ACM-KIT...

The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2024· Steris Corporation

Recalled Item: Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide...

The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2024· Hologic Inc

Recalled Item: Horizon X-Ray Bone Densitometer (DXA) Models: Horizon-A Recalled by Hologic...

The Issue: Non-conformance pertains to electromagnetic compatibility requirements...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2024· Steris Corporation

Recalled Item: Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups...

The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2024· Steris Corporation

Recalled Item: Hookup Model/Catalog Number: 2-8-540HAN Product Description: Hookups provide...

The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2024· Steris Corporation

Recalled Item: Hookup Model/Catalog Number: 2-8-540 Product Description: Hookups provide...

The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...

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

Class II — Potential Health HazardOngoing
FoodJune 13, 2024· Totally Cool, Inc.

Recalled Item: Dolcezza Peanut Butter Stracciatella Gelato 16 fl oz/1 pint Recalled by...

The Issue: Possible contamination with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund