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. 2,689 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,689 in last 12 months

Showing 1236112380 of 53,342 recalls

Medical DeviceJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: AT HOME MARIJUANA TEST STRIP Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: SKYN ORIGINAL NON LATEX CONDOM 12CT Recalled by Family Dollar Stores, Llc....

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ Recalled by Family Dollar Stores, Llc....

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing
FoodJune 22, 2022· Blount Fine Foods Corporation

Recalled Item: Panera Bread at Home Southwest Corn Chowder Recalled by Blount Fine Foods...

The Issue: Contains undeclared wheat

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 22, 2022· ASO LLC

Recalled Item: (1) CVS Health Sterile Surgical Pads Recalled by ASO LLC Due to The product...

The Issue: The product falls apart during handling after removal from its primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2022· Intuitive Surgical, Inc.

Recalled Item: The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit...

The Issue: Due to preventative maintenance (PM) not being performed on E-100 generators...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2022· Meridian Bioscience Inc

Recalled Item: Revogene Recalled by Meridian Bioscience Inc Due to When a run is aborted,...

The Issue: When a run is aborted, the cooling period protection does not occur and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2022· Integra LifeSciences Corp.

Recalled Item: CereLink ICP Monitor Recalled by Integra LifeSciences Corp. Due to Integra...

The Issue: Integra has received complaints associated with ICP readings drifting to -50...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 22, 2022· Randox Laboratories Ltd.

Recalled Item: Randox Cholesterol- For the quantitative in vitro determination of...

The Issue: Product fails to meet the performance claims quoted on the kit insert:...

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

Class II — Potential Health HazardOngoing
DrugJune 21, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules Recalled by SUN...

The Issue: Superpotent Drug: Out of specification for assay at the 12-month timepoint.

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules Recalled by SUN...

The Issue: Superpotent Drug: Out of specification for assay at the 12-month timepoint.

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: cGMP - Water leakage

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 21, 2022· Tarts A La Carte, LLC dba Blazo Pie shoppe LLC

Recalled Item: 9-inch pie Blazos Pie Shoppe Chocolate Peanut Butter Cream Pie Recalled by...

The Issue: Blazos Pie Shoppe Peanut Butter Cream Pie, Chocolate Peanut Butter Cream Pie...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 21, 2022· Tarts A La Carte, LLC dba Blazo Pie shoppe LLC

Recalled Item: 10 oz Blazos Pie Shoppe Peanut Butter Cream Cup () Recalled by Tarts A La...

The Issue: Blazos Pie Shoppe Peanut Butter Cream Pie, Chocolate Peanut Butter Cream Pie...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 21, 2022· Food Entrepreneur Accelerator and Startup Terminal, DBA FEAST Detroit

Recalled Item: Blue Kuna Taste of Devil's Night Heat Infused BBQ Sauce Recalled by Food...

The Issue: The product was mislabeled as Vegan Product but contains anchovies

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 21, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...

The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...

The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2022· Touch US Llc

Recalled Item: etouchus Recalled by Touch US Llc Due to Device was marketed without FDA...

The Issue: Device was marketed without FDA 510(k) clearance or a PMA.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2022· NuVasive Inc

Recalled Item: Description/Part: Simplify Disc Size 1 Recalled by NuVasive Inc Due to...

The Issue: Cervical artificial disc Unique Device Identifier (UDI) barcodes contain the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2022· Bard Access Systems, Inc.

Recalled Item: Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit...

The Issue: BD Intraosseous Needle Kits may exhibit: 1) Increased force required to...

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

Class I — Serious Health HazardOngoing