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. 2,563 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,563 in last 12 months

Showing 2492124940 of 53,342 recalls

FoodOctober 18, 2018· Trident Seafoods Corporation

Recalled Item: Kroger brand. Frozen non-ready to eat Alaskan Salmon Bites Recalled by...

The Issue: Frozen non-ready to eat Alaskan Salmon Bites, Kroger brand, are recalled due...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 18, 2018· Harvest Food Group

Recalled Item: Path of Life All Natural Southwest Quinoa Recalled by Harvest Food Group Due...

The Issue: Products recalled due to potential contamination with Listeria monocytogenes...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 18, 2018· Harvest Food Group

Recalled Item: Signature Select Mexican Style Roasted Corn Recalled by Harvest Food Group...

The Issue: Products recalled due to potential contamination with Listeria monocytogenes...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 18, 2018· H J Harkins Company Inc dba Pharma Pac

Recalled Item: GENTAMICIN OPTH-SOL 5ml Compare: Garamycin. 5-mL plastic dropper bottle...

The Issue: Presence of Particulate Matter: Crystalline particles were noticed by...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 18, 2018· Promise Pharmacy LLC

Recalled Item: Prednisolone and Gatifloxacin Ophthalmic Solution Recalled by Promise...

The Issue: Presence of precipitate

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16 Slice (Air) Recalled by Philips Medical Systems (Cleveland)...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 6 Slice (Air) Recalled by Philips Medical Systems (Cleveland) Inc...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· EUROTROL INC

Recalled Item: HemoTrol Level 3- In Vitro Diagnostic Hematology quality control mixture....

The Issue: Incorrect measurement results caused by microbial contamination of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 10 Slice (Air) Recalled by Philips Medical Systems (Cleveland)...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Beckman Coulter Inc.

Recalled Item: iChem VELOCITY Urine Chemistry Strips Recalled by Beckman Coulter Inc. Due...

The Issue: Falsely elevated (false positive) urobilinogen patient results due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 40 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16 Slice (Power) Recalled by Philips Medical Systems (Cleveland)...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· EUROTROL INC

Recalled Item: HemoTrol Level 2- In Vitro Diagnostic Hematology quality control mixture...

The Issue: Incorrect measurement results caused by microbial contamination of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-400 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-406 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-401 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-RFP-454 Recalled by NxStage Medical, Inc....

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-404 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· Richard Wolf GmbH

Recalled Item: Richard Wolf Bronchoscope Tubes Recalled by Richard Wolf GmbH Due to There...

The Issue: There is a potential deficiency of the TEXAS Bronchoscope Tube product. The...

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

Class II — Potential Health HazardOngoing