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. 1,849 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
1,849 in last 12 months

Showing 3166131680 of 52,120 recalls

Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10.5MM Product Number:...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9.5MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· King Systems Corp. dba Ambu, Inc.

Recalled Item: UNIVERSAL FLEX2 BREATHING CIRCUIT Recalled by King Systems Corp. dba Ambu,...

The Issue: Potential for leak test failures.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Ultimax Digital Fluoroscopic X-Ray System...

The Issue: The issue was identified as a firmware problem with the generator.

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

Class II — Potential Health HazardOngoing
DrugMarch 15, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...

The Issue: Failed Dissolution Specifications; 9 month long term stability

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 15, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by Sun Pharmaceutical Industries,...

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 14, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Connect Diabetes Management App versions 2.0.0 Recalled by Roche...

The Issue: A program error (bug) in the Bolus Advisor feature, which could result in...

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

Class II — Potential Health HazardOngoing
FoodMarch 14, 2017· J & J Distributing Company

Recalled Item: Mix General Tso Chik Recalled by J & J Distributing Company Due to J&J...

The Issue: J&J Distributing Company reported that a small amount of shred carrots were...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2017· J & J Distributing Company

Recalled Item: Detox Salad Recalled by J & J Distributing Company Due to J&J Distributing...

The Issue: J&J Distributing Company reported that a small amount of shred carrots were...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2017· J & J Distributing Company

Recalled Item: Kowalski's Markets Recalled by J & J Distributing Company Due to J&J...

The Issue: J&J Distributing Company reported that a small amount of shred carrots were...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2017· J & J Distributing Company

Recalled Item: Kowalski's Markets Recalled by J & J Distributing Company Due to J&J...

The Issue: J&J Distributing Company reported that a small amount of shred carrots were...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2017· J & J Distributing Company

Recalled Item: Shred Carrots Recalled by J & J Distributing Company Due to J&J Distributing...

The Issue: J&J Distributing Company reported that a small amount of shred carrots were...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2017· J & J Distributing Company

Recalled Item: Kowalski's Markets Recalled by J & J Distributing Company Due to J&J...

The Issue: J&J Distributing Company reported that a small amount of shred carrots were...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2017· J & J Distributing Company

Recalled Item: Cub Foods (Fresh) Recalled by J & J Distributing Company Due to J&J...

The Issue: J&J Distributing Company reported that a small amount of shred carrots were...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2017· J & J Distributing Company

Recalled Item: Rainbow Coleslaw Recalled by J & J Distributing Company Due to J&J...

The Issue: J&J Distributing Company reported that a small amount of shred carrots were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 14, 2017· Hans Pausch Rontgengeratebau Gmbh

Recalled Item: Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040...

The Issue: During patient interventions with the urology table the radiation is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2017· Valeant Pharmacueticals International

Recalled Item: Small Particle Aerosol Generator Model SPAG-2 6000 Series (SPAG-2). The...

The Issue: SPAG-2 unit nebulizers from Lot J0571670RA were tested at Next Breath for...

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

Class II — Potential Health HazardOngoing