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. 2,647 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,647 in last 12 months

Showing 1594115960 of 53,342 recalls

Medical DeviceJune 11, 2021· Medtronic Heart Valves Division

Recalled Item: CoreValve Evolut PRO Delivery Catheter System Recalled by Medtronic Heart...

The Issue: Due to reports of actuator separation for various delivery catheter systems....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2021· Medtronic Heart Valves Division

Recalled Item: CoreValve Evolut R Delivery Catheter System Recalled by Medtronic Heart...

The Issue: Due to reports of actuator separation for various delivery catheter systems....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2021· Medtronic Heart Valves Division

Recalled Item: CoreValve Evolut PRO PLUS Delivery Catheter System Recalled by Medtronic...

The Issue: Due to reports of actuator separation for various delivery catheter systems....

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

Class II — Potential Health HazardOngoing
DrugJune 10, 2021· CIPLA

Recalled Item: Solifenacin Succinate Tablets Recalled by CIPLA 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 DeviceJune 10, 2021· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Arjo Citadel beds originally assembled with the IndiGo modules during...

The Issue: The IndiGo power cord might wear during use which could lead to its damage,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...

The Issue: There is a potential for >10% under-recovery on Activated Alanine...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for 15%...

The Issue: There is a potential for 15% under-recovery on Activated Alanine...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...

The Issue: There is a potential for >10% under-recovery on Activated Alanine...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...

The Issue: There is a potential for >10% under-recovery on Activated Alanine...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· GE OEC Medical Systems, Inc

Recalled Item: OEC 3D Imaging Recalled by GE OEC Medical Systems, Inc Due to There is a...

The Issue: There is a potential that the coin cell battery used to monitor X-Ray tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Merit Medical Systems, Inc.

Recalled Item: basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Recalled by...

The Issue: Due to a design issue, inflation syringe handle separating from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· GE OEC Medical Systems, Inc

Recalled Item: OEC Elite mobile C-arm - Product Usage: intended to provide Recalled by GE...

The Issue: There is a potential that the coin cell battery used to monitor X-Ray tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Mercedes Medical, Inc.

Recalled Item: Lingen SAMPLE Disposable Virus Sampling Kit pack Recalled by Mercedes...

The Issue: No 510(k) clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Mercedes Medical, Inc.

Recalled Item: Lingen Disposable Virus Sampling Kit Recalled by Mercedes Medical, Inc. Due...

The Issue: No 510(k) clearance

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

Class II — Potential Health HazardOngoing
DrugJune 9, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDAs...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline)Tablets Recalled by Pfizer Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDAs...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2021· Genentech Inc

Recalled Item: Xolair (omalizumab) Injection Recalled by Genentech Inc Due to Failed...

The Issue: Failed Stability Specifications: Out of Specification results of Polysorbate...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 9, 2021· Olympus Corporation of the Americas

Recalled Item: Gyrus Acmi PKS Omni 5mm/33cm-intended for the electrosurgical coagulation...

The Issue: Expired adhesive used as an electrical insulation barrier and as a secondary...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2021· Cardinal Health 200, LLC

Recalled Item: Infant Heel Warmer with Attachment Tab Recalled by Cardinal Health 200, LLC...

The Issue: A caution statement is being added to remind the user to activate away from...

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

Class II — Potential Health HazardOngoing