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. 2,478 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,478 in last 12 months

Showing 2638126400 of 52,120 recalls

Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 360 mm Recalled by Zimmer...

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 DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 300 mm Recalled by Zimmer...

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 DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 420 mm Recalled by Zimmer...

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 DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 400 mm Recalled by Zimmer...

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 DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 320 mm Recalled by Zimmer...

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 DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 125¿ 11 mm x 400 mm Recalled by Zimmer...

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
DrugJuly 17, 2018· A-S Medication Solutions LLC.

Recalled Item: Valsartan Tablets Recalled by A-S Medication Solutions LLC. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2018· A-S Medication Solutions LLC.

Recalled Item: Valsartan and Hydrochlorothiazide Tablets Recalled by A-S Medication...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2018· A-S Medication Solutions LLC.

Recalled Item: Valsartan and Hydrochlorothiazide Tablets Recalled by A-S Medication...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2018· A-S Medication Solutions LLC.

Recalled Item: Valsartan Tablets Recalled by A-S Medication Solutions LLC. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 16, 2018· AMPI

Recalled Item: AMPI Whey Powder Recalled by AMPI Due to Potential Salmonella Contamination

The Issue: Whey powder may have the potential to be contaminated with Salmonella.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 16, 2018· General Mills, Inc

Recalled Item: Cheerios Protein Oats & Honey Recalled by General Mills, Inc Due to...

The Issue: Cheerios Protein Oats and Honey cereal may be contaminated with Salmonella.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 16, 2018· D & D Foods, Inc.

Recalled Item: Hy-Vee Spring Pasta Salad packaged in the following containers: 1) Recalled...

The Issue: Outbreak of Salmonella Sandiego and Salmonella enterica subspecies IIIb...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 9 F FDXD Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS CV Recalled by Philips Electronics North America Corporation Due to...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD1O C Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Poly C- DMCP-Visub(H3000) Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: RAPIDLab 1245 Blood Gas Analyzer Recalled by Siemens Healthcare Diagnostics,...

The Issue: Therapeutic levels (1mg/mL and 2mg/mL) of Hydroxocobalamin may interfere...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: RAPIDLab 1265 Blood Gas Analyzer Recalled by Siemens Healthcare Diagnostics,...

The Issue: Therapeutic levels (1mg/mL and 2mg/mL) of Hydroxocobalamin may interfere...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 15-12 (mono) Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing