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. 2,645 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,645 in last 12 months

Showing 1678116800 of 53,342 recalls

Medical DeviceMarch 15, 2021· Medtronic Minimed

Recalled Item: MiniMed 670G Insulin Pump: Models: PUMP MMT-1740KX 670G V6.3 SF MG CLIN...

The Issue: Due to a software design issue, under certain conditions, a software fault...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2021· Medtronic Minimed

Recalled Item: MiniMed 780G Insulin Pump: Models: PUMP MMT-1885 MM780G 6.5V BLE MMOL...

The Issue: Due to a software design issue, under certain conditions, a software fault...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2021· St. Jude Medical, Cardian Rhythm Management Division

Recalled Item: ENDURITY Pulse Generator **** SN ********* St. Jude Medical Recalled by St....

The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2021· St. Jude Medical, Cardian Rhythm Management Division

Recalled Item: ASSURITY Pulse Generator **** SN ********* ST. JUDE MEDICAL Recalled by St....

The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2021· B. Braun Medical, Inc.

Recalled Item: Filtered Triple-Leg Extension Set - Intravascular administration set....

The Issue: BBMI has identified through complaints the potential for the extension set...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2021· Medline Industries Inc

Recalled Item: Diluent Recalled by Medline Industries Inc Due to Possible false negative or...

The Issue: Possible false negative or false positive results due to the product being...

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2021· Ferring Pharmaceuticals Inc

Recalled Item: ZOMA-Jet 10 Demonstration Kit Recalled by Ferring Pharmaceuticals Inc Due to...

The Issue: Defective Delivery System: customer complaints concerning the injector pen...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2021· Ferring Pharmaceuticals Inc

Recalled Item: ZOMA-Jet 5 Demonstration Kit Recalled by Ferring Pharmaceuticals Inc Due to...

The Issue: Defective Delivery System: customer complaints concerning the injector pen...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2021· Breckenridge Pharmaceutical, Inc

Recalled Item: Omeprazole Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2021· Sagent Pharmaceuticals Inc

Recalled Item: Phenylephrine HCl Injection Recalled by Sagent Pharmaceuticals Inc Due to...

The Issue: Lack of Assurance of Sterility: customer complaints of loose crimped vial...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 11, 2021· Mindo Chocolate Makers LLC

Recalled Item: Mindo COFFEE TOFFEE CHOCOLATE BAR Recalled by Mindo Chocolate Makers LLC Due...

The Issue: Undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2021· LIEBEL-FLARSHEIM COMPANY LLC

Recalled Item: HydraVision Digital Imaging System Product ID/Reorder Number: 705559 (65KW)...

The Issue: Failure to comply with the performance standard for fluoroscopy systems. Per...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2021· Stryker Spine

Recalled Item: Tritanium X TL Instruments - intervertebral fusion device with bone graft...

The Issue: Stryker identified non-conforming instruments that are components of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2021· Arthrex, Inc.

Recalled Item: Tibial Opening Wedge Osteotomy Plate Recalled by Arthrex, Inc. Due to It was...

The Issue: It was discovered that five AR-13200ST-15.0 parts were processed as...

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

Class II — Potential Health HazardOngoing
DrugMarch 10, 2021· China Gel Inc

Recalled Item: CHINA-GEL WHITE (Camphor 3.00% Recalled by China Gel Inc Due to CGMP...

The Issue: CGMP deviations: Product being recalled as it was made in the same facility...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2021· China Gel Inc

Recalled Item: CHINA_GEL (Camphor 3.00% Recalled by China Gel Inc Due to CGMP deviations:...

The Issue: CGMP deviations: Product being recalled as it was made in the same facility...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2021· China Gel Inc

Recalled Item: aulief (Organic Camphor 3.00% Organic Menthol 5.00%) Recalled by China Gel...

The Issue: CGMP deviations: Product being recalled as it was made in the same facility...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2021· Sanit Technologies, LLC dba Durisan

Recalled Item: Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing...

The Issue: Microbial Contamination of Non-Sterile Products: firm's internal testing...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 10, 2021· Sanit Technologies, LLC dba Durisan

Recalled Item: Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizer...

The Issue: CGMP Deviations: lots recalled due to CGMP deviations because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2021· Sanit Technologies, LLC dba Durisan

Recalled Item: Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing...

The Issue: CGMP Deviations: lots recalled due to CGMP deviations because they were...

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

Class II — Potential Health HazardOngoing
Refund