Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,589 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,589 in last 12 months

Showing 1518115200 of 29,186 recalls

Medical DeviceOctober 2, 2018· Pfizer Inc.

Recalled Item: Thermacare Muscle Pain Therapy HeatWraps: a) b) Recalled by Pfizer Inc. Due...

The Issue: The firm received complaints of the wrap coming apart and leaking granular...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Pfizer Inc.

Recalled Item: Thermacare HEATWRAPS JOINT PAIN THERAPY Recalled by Pfizer Inc. Due to The...

The Issue: The firm received complaints of the wrap coming apart and leaking granular...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 125 Deg 12x165mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 130 Deg 10x165mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 130 Deg 11x300mm Recalled by Zimmer Biomet,...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 9x165mm Recalled by Zimmer Biomet,...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 11x300mm Recalled by Zimmer Biomet,...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 125 Deg 10x165mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left Deg 9x300mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 130 Deg 12x165mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Straumann Manufacturing, Inc.

Recalled Item: Neodent¿ GM Mini Conical Abutment - Product Usage: Mini Conical Recalled by...

The Issue: Laser engraved label does not match with the item in the package

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2018· Comet Technologies Usa Inc

Recalled Item: YXLON Cougar Cabinet X-Ray System Product Usage: The products are Recalled...

The Issue: Failure to meet the requirement of the performance standard for cabinet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2018· Comet Technologies Usa Inc

Recalled Item: YXLON Cheetah cabinet X-Ray System Product Usage: The products are Recalled...

The Issue: Failure to meet the requirement of the performance standard for cabinet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Countersink 1.7mm Recalled by TriMed Inc. Due to The epoxy on Apex...

The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Peg Guide Extender Recalled by TriMed Inc. Due to The spring on the...

The Issue: The spring on the PEG-Extender can rust due to the type of steel used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Locking Drill Guide Recalled by TriMed Inc. Due to The epoxy on Apex...

The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Hex Driver 1.2 Recalled by TriMed Inc. Due to The epoxy on Apex...

The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Wrist Hook Dorsal Impactor Recalled by TriMed Inc. Due to The WHD/WHV...

The Issue: The WHD/WHV impactors can rust over time due to an improper manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...

The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-900Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience has...

The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...

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

Class II — Potential Health HazardOngoing