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. 2,666 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,666 in last 12 months

Showing 1378113800 of 53,342 recalls

Medical DeviceFebruary 17, 2022· Deerfield Imaging, Inc.

Recalled Item: Trumpf Mount Clamp Assembly (table adapter component) Recalled by Deerfield...

The Issue: Reports have been received that after normal or routine lateral forces are...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2022· Kaneka America Corp

Recalled Item: LIPOSORBER System Recalled by Kaneka America Corp Due to Labeling change to...

The Issue: Labeling change to due to the risk of severe anaphylactoid reactions...

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

Class II — Potential Health HazardOngoing
DrugFebruary 16, 2022· TCP HRB ACQUISITON LLC

Recalled Item: Sure Unscented Anti-perspirant Deodorant Aerosol (Aluminum Chlorohydrate...

The Issue: Chemical contamination: Presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 16, 2022· TCP HRB ACQUISITON LLC

Recalled Item: Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%)...

The Issue: Chemical contamination: Presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 16, 2022· TCP HRB ACQUISITON LLC

Recalled Item: Sure Regular Antiperspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%)...

The Issue: Chemical contamination: Presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 16, 2022· Macleods Pharma Usa Inc

Recalled Item: Olanzapine Tablets Recalled by Macleods Pharma Usa Inc Due to cGmp Deviations

The Issue: cGmp Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 16, 2022· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter IRISpec CA/CB/CC control Recalled by Beckman Coulter, Inc....

The Issue: IRISpec CA failures for glucose.

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

Class III — Low RiskOngoing
DrugFebruary 15, 2022· ANI Pharmaceuticals, Inc.

Recalled Item: Pyrazinamide Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2022· Macleods Pharma Usa Inc

Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Macleods Pharma Usa...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2022· ANI Pharmaceuticals, Inc.

Recalled Item: Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2022· ANI Pharmaceuticals, Inc.

Recalled Item: Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2022· ANI Pharmaceuticals, Inc.

Recalled Item: Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2022· ANI Pharmaceuticals, Inc.

Recalled Item: Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2022· Meridian Bioscience Inc

Recalled Item: Revogene Recalled by Meridian Bioscience Inc Due to The photomultiplier...

The Issue: The photomultiplier tube, may have compromised functionality in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2022· Ion Beam Applications S.A.

Recalled Item: ProteusPLUS and ProteusONE- designed to produce and deliver a proton...

The Issue: When resuming from a beam pause, the Proton Therapy System does not verify...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2022· Draeger Medical, Inc.

Recalled Item: Evita V500 Ventilator with Software 2.51.01 and Lower - intended Recalled by...

The Issue: Cybersecurity Improvement Action-not equipped against potential cyber...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2022· Cook Medical Incorporated

Recalled Item: Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach Recalled by...

The Issue: IFU update includes an update to the Device description, Intended...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 14, 2022· Cook Medical Incorporated

Recalled Item: Cook Celect PlatinumVena Cava Filter Set Catalog Number/GPN:...

The Issue: IFU update includes an update to the Device description, Intended...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 14, 2022· Draeger Medical, Inc.

Recalled Item: Babylog VN500 Ventilator with Software 2.51.01 and Lower- intended for...

The Issue: Cybersecurity Improvement Action-not equipped against potential cyber...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2022· Cytocell Ltd.

Recalled Item: Cytocell 8 Square Template Slides (Glass)- microscope slides : PCN008...

The Issue: Labelled with an incorrect expiry date on the outer label with an extended...

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

Class III — Low RiskOngoing