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. 1,057 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
1,057 in last 12 months

Showing 17661–17680 of 53,342 recalls

Medical DeviceNovember 18, 2020· Shimadzu Medical Systems

Recalled Item: Bransist Safire Recalled by Shimadzu Medical Systems Due to The firm has...

The Issue: The firm has identified a problem with the control software for the celling...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Philips North America Llc

Recalled Item: Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended...

The Issue: Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Zimmer Biomet, Inc.

Recalled Item: Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System Recalled by...

The Issue: Zimmer Biomet is conducting a medical device correction to update the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus LS - Manual Defibrillator Recalled by Remote Diagnostic Technologies...

The Issue: A software error was detected within software version 1.3.4 for the Tempus...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
DrugNovember 17, 2020· Golden State Medical Supply Inc.

Recalled Item: ARIPIPRAZOLE TABLETS Recalled by Golden State Medical Supply Inc. Due to...

The Issue: FAILED DISSOLUTION SPECIFICATIONS: Possibility of out-of-specification (OOS)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 17, 2020· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: RiteAid Pharmacy RIngworm Cream Recalled by Taro Pharmaceuticals U.S.A.,...

The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 17, 2020· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Kroger Jock Itch Cream Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 17, 2020· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Kroger Athlete's Foot Cream Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 17, 2020· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: TopCare Health Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 17, 2020· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: CVS Health Athlete's Foot Cream Recalled by Taro Pharmaceuticals U.S.A.,...

The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 17, 2020· BASF Corporation

Recalled Item: Kollidon CL-M Crospovidone Ph.Eur.Type B Recalled by BASF Corporation Due to...

The Issue: Cross contamination: the excipient was found to be contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 17, 2020· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Athlete's Foot Cream Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 17, 2020· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Best Choice Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 17, 2020· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Kaiser Permanente Clotrimazole Cream USP Recalled by Taro Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...

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

Class II — Potential Health HazardOngoing
Refund