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. 2,742 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,742 in last 12 months

Showing 16411660 of 53,342 recalls

Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Brilliance 16 Power Recalled...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity CT 728326 Recalled...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity Core128 Recalled...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Brilliance iCT SP Recalled...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 900 COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 690T COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
FoodAugust 12, 2025· Bakers Authority LLC

Recalled Item: Baker's Authority Three Seed Mix Recalled by Bakers Authority LLC Due to...

The Issue: Product label does not list ingredients including major food allergen:...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 12, 2025· Bakers Authority LLC

Recalled Item: Baker's Authority Everything Bagel Mix Recalled by Bakers Authority LLC Due...

The Issue: Product label does not list ingredients including major food allergen:...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 12, 2025· Bakers Authority LLC

Recalled Item: Baker's Authority Graham Cracker Meal Recalled by Bakers Authority LLC Due...

The Issue: Product label does not list ingredients including major food allergens:...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 12, 2025· VIONA PHARMACEUTICALS INC

Recalled Item: Tavaborole Topical Solution 5% Recalled by VIONA PHARMACEUTICALS INC Due to...

The Issue: Discoloration

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 12, 2025· Max Mobility LLC

Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...

The Issue: Due to a faulty electrical connection between the speed control Dial and the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 12, 2025· Max Mobility LLC

Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...

The Issue: Due to a faulty electrical connection between the speed control Dial and the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 12, 2025· Max Mobility LLC

Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...

The Issue: Due to a faulty electrical connection between the speed control Dial and the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 12, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Pheno. Image-Intensified Flouroscopic X-Ray System. Recalled by...

The Issue: Limited system movements after startup .

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

Class II — Potential Health HazardOngoing
DrugAugust 11, 2025· Lannett Company Inc.

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by Lannett Company Inc. Due to...

The Issue: Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 11, 2025· Agilent Technologies Denmark ApS

Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...

The Issue: Their is the potential for weak staining which may result in false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2025· Agilent Technologies Denmark ApS

Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...

The Issue: Their is the potential for weak staining which may result in false negative...

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

Class II — Potential Health HazardOngoing