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 1640116420 of 53,342 recalls

FoodApril 16, 2021· Creative Foods Inc

Recalled Item: Bueno Coffee Substitute Creamy Hazelnut Recalled by Creative Foods Inc Due...

The Issue: Bueno Coffee Substitute Creamy Hazelnut product contains undeclared hazelnut...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 16, 2021· Luminex Corporation

Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Impacted lot may...

The Issue: Impacted lot may leak inside the ARIES instrument.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2021· Aesculap Implant Systems LLC

Recalled Item: PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU Recalled by...

The Issue: Malfuncton-Implant did not deploy successfully may necessitate the need for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2021· Aesculap Implant Systems LLC

Recalled Item: PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-000001-13...

The Issue: Malfuncton-Implant did not deploy successfully may necessitate the need for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2021· BioFire Diagnostics, LLC

Recalled Item: FilmArray Pneumonia Panel (Penumo) Recalled by BioFire Diagnostics, LLC Due...

The Issue: Elevated rates of false positive/false negative and control failures while...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2021· Hardy Diagnostics

Recalled Item: Quickslide GramPro 1 Automated Gram Stanier is a microscope slide stainer....

The Issue: Instruments were assembled and serviced using a defective lot of tubing,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2021· Draeger Medical, Inc.

Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...

The Issue: Three separate and unrelated problems attributed to the software used in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2021· Draeger Medical, Inc.

Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...

The Issue: Three separate and unrelated problems attributed to the software used in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2021· Draeger Medical, Inc.

Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...

The Issue: Three separate and unrelated problems attributed to the software used in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2021· Draeger Medical, Inc.

Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...

The Issue: Three separate and unrelated problems attributed to the software used in the...

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

Class II — Potential Health HazardOngoing
DrugApril 15, 2021· Grace Healthcare Medical, Inc

Recalled Item: Oxygen Recalled by Grace Healthcare Medical, 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 DeviceApril 15, 2021· Vygon U.S.A.

Recalled Item: Vygon Dressing Change w/ Maxiswab - Product Usage: Custom Dressing Change...

The Issue: Compromised sterile barriers due to the Tyvek Lid not properly adhering to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2021· Flower Orthopedics Corporation

Recalled Item: T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits Recalled...

The Issue: Cannulated Screwdrivers may break at the driver tip along the shaft, near...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2021· Haag-Streit USA Inc

Recalled Item: Eyesuite 9.3.1 software Recalled by Haag-Streit USA Inc Due to Examination...

The Issue: Examination data and patient name may be mixed up when printing or...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2021· Boston Scientific Corporation

Recalled Item: UpsylonTM Y Mesh Kit with Colpassist Vaginal Positioning Device - Recalled...

The Issue: Potential for pinholes (sterile barrier breach) on the edge of the pouch to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2021· Boston Scientific Corporation

Recalled Item: Colpassist Vaginal Positioning Device - Product Usage: intended for use...

The Issue: Potential for pinholes (sterile barrier breach) on the edge of the pouch to...

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

Class II — Potential Health HazardOngoing
DrugApril 14, 2021· Fresenius Medical Care, North America

Recalled Item: Delflex Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Labeling; Label Mix-up; 4.25% DEXTROSE bag was found inside a 1.5% DEXTROSE box.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2021· Blount Fine Foods Corporation

Recalled Item: Panera Lobster Bisque Recalled by Blount Fine Foods Corporation Due to...

The Issue: Lobster bisque contains undeclared noodle with egg ingredient.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 14, 2021· Dutch Ophthalmic USA, Inc.

Recalled Item: Illuminated Stepped Laser Probe Curved-for use in combination with 23G...

The Issue: Barcode label extended expiration date. Barcode located at the short side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2021· Radiometer Medical ApS

Recalled Item: E3800 PC Units (spare parts) Recalled by Radiometer Medical ApS Due to Due...

The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...

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

Class II — Potential Health HazardOngoing