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. 2,632 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,632 in last 12 months

Showing 1856118580 of 53,342 recalls

DrugJuly 23, 2020· Real Clean Distribuciones SA de CV

Recalled Item: BORN BASIC. Recalled by Real Clean Distribuciones SA de CV Due to CGMP...

The Issue: CGMP Deviations: Born Basic Anti Bac was found to be below the label claim...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2020· Real Clean Distribuciones SA de CV

Recalled Item: scent theory KEEP IT CLEAN Recalled by Real Clean Distribuciones SA de CV...

The Issue: CGMP Deviations: Other products were recalled because they were manufactured...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 23, 2020· Upspring,ltd

Recalled Item: UpSpring Baby Iron + Immunity MULTI + IRON + ZINC Recalled by Upspring,ltd...

The Issue: May contain undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 23, 2020· Remel Europe Ltd.

Recalled Item: Thermo Scientific Remel Bordetella pertussis Agglutinating Serum Product...

The Issue: Thermo Scientific" Remel" Bordetella pertussis Agglutinating Serum...

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

Class II — Potential Health HazardOngoing
DrugJuly 22, 2020· Fresenius Kabi USA, LLC

Recalled Item: Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Recalled by Fresenius...

The Issue: Cross Contamination with other products: trace amounts of lidocaine

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 22, 2020· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost R90 Software Version R1.0 and R1.1 Recalled by Philips Medical...

The Issue: Philips has become aware of a software issue, where the kV and mA values are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2020· Smith & Nephew Orthopaedics AG

Recalled Item: POLARSTEM COLLAR Reamer Guide Recalled by Smith & Nephew Orthopaedics AG Due...

The Issue: Multiple lots being recalled due to a product design issue

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

Class II — Potential Health HazardOngoing
DrugJuly 21, 2020· Ferring Pharmaceuticals Inc

Recalled Item: STIMATE (desmopressin acetate) Nasal Spray1.5 mg/mL Recalled by Ferring...

The Issue: Superpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 21, 2020· Ferring Pharmaceuticals Inc

Recalled Item: Desmopressin Acetate Nasal Spray 10 mcg/0.1 mL Recalled by Ferring...

The Issue: Superpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 21, 2020· Ferring Pharmaceuticals Inc

Recalled Item: DDAVP Nasal Spray (desmopressin acetate) 10 mcg/0.1 mL Recalled by Ferring...

The Issue: Superpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 21, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Mibelas 24 Fe (norethindrone acetate and ethinyl estradiol tablets and...

The Issue: Failed Impurities/Degradation Specifications: Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 21, 2020· BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA

Recalled Item: Ezycare Face Mask Recalled by BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA...

The Issue: Disposable face masks labeled as non-medical were distributed to customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-CH EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMT ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing