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. 2,065 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,065 in last 12 months

Showing 62216240 of 53,342 recalls

FoodApril 10, 2024· FEEL GOOD FOODS INC

Recalled Item: Cream Cheese Stuffed Plain Mini Bagels Recalled by FEEL GOOD FOODS INC Due...

The Issue: Contains undeclared gluten

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2024· Imprimis NJOF, LLC

Recalled Item: Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free...

The Issue: Out of specification for assay

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

Class III — Low RiskOngoing
Refund
FoodApril 10, 2024· FEEL GOOD FOODS INC

Recalled Item: Cream Cheese Stuffed Everything Mini Bagels Recalled by FEEL GOOD FOODS INC...

The Issue: Contains undeclared gluten

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 9, 2024· Sophysa S.A.

Recalled Item: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit...

The Issue: An increase in claims related to leakage of cerebrospinal fluid (CSF) from...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· QUIDELORTHO

Recalled Item: VITROS Immunodiagnostic Products Free T3 Reagent Pack-IVD is for the...

The Issue: T3 Reagent Packs used with Free T3 Calibrators may produce positively biased...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· Baxter Healthcare Corporation

Recalled Item: Spectrum IQ Infusion pump Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is a potential for cracks on the mount of the front panel of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· QUIDELORTHO

Recalled Item: VITROS Immunodiagnostic Products Free T3 Calibrators-IVD are for use with...

The Issue: Free T3 Calibrators used with T3 Reagent Packs may produce positively biased...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· GE Medical Systems Information Technologies Inc

Recalled Item: GE HealthCare CRITIKON ONE-CUF blood pressure cuffs Recalled by GE Medical...

The Issue: Use of the blood pressure cuffs could result in inaccurate non-invasive...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· Sophysa S.A.

Recalled Item: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit...

The Issue: An increase in claims related to leakage of cerebrospinal fluid (CSF) from...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) CONTINUOUS BLOCK Recalled by MEDLINE...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: Novalung sensor box is a component of the Novalung Console Recalled by...

The Issue: Issue related to Novalung sensor box, which is a component of the Novalung...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) NEPHROLOGY PACK Recalled by MEDLINE...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 Recalled by...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2024· Vyaire Medical, Inc.

Recalled Item: Vyaire Medical GmbH Recalled by Vyaire Medical, Inc. Due to Potential of the...

The Issue: Potential of the nozzle separating during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2024· HeartSine Technologies Ltd

Recalled Item: HeartSine samaritan PAD (Public Access Defibrillator) Recalled by HeartSine...

The Issue: Automated external defibrillators have a manufacturing issue that could...

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

Class II — Potential Health HazardOngoing
FoodApril 8, 2024· D-lo's Gourmet Cheesecake

Recalled Item: D-LO's Delightful Gourmet Cheesecake Recalled by D-lo's Gourmet Cheesecake...

The Issue: Undeclared wheat, soy, colors (yellow 5 and blue 1), incomplete contains...

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

Class I — Serious Health HazardOngoing
Refund