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. 1,749 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
1,749 in last 12 months

Showing 4858148600 of 52,120 recalls

FoodMarch 28, 2013· Rich Products Corp

Recalled Item: Farm Rich Better For You Pizza Dippers-Pizza Dough made with Recalled by...

The Issue: Products potentially contaminated with E. coli O121.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· All One, Inc.

Recalled Item: all One Original Formula Multiple Vitamin & Mineral Powder dietary...

The Issue: Product label misprinted to include claim of "No Dairy", even though milk is...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 28, 2013· Rich Products Corp

Recalled Item: Mozzarella Bites distributed under the following labels: Farm Rich Cheese...

The Issue: Products potentially contaminated with E. coli O121.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Dark Peanut Butter Cup Recalled by NuGo Nutrition HQ Due to Undeclared Milk

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Slim Crunchy Peanut Butter Recalled by NuGo Nutrition HQ Due to...

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Dark Mint Chocolate Chip Recalled by NuGo Nutrition HQ Due to...

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Dark Mocha Recalled by NuGo Nutrition HQ Due to Undeclared Milk

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Free Carrot Cake Recalled by NuGo Nutrition HQ Due to Undeclared Milk

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: OraTape Absorbable Collagen Wound Dressing for Dental Surgery The Absorbable...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Dural Graft Matrix DuraGen¿ Dural Graft Matrix is an absorbable Recalled by...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: CollaCote Absorbable Collagen Wound Dressing for Dental Surgery The...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: DuraGen Plus Dural Regeneration Matrix DuraGen Plus Adhesion Barrier Matrix...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Absorbable Collagen Sponge Provided As Intermediate to Another Company...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Suturable DuraGen Dural Regenerative Matrix Suturable DuraGen Dural...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Abbott Molecular

Recalled Item: The CEP 8 SpectrumGreen (SG) ASR Probe Kit Recalled by Abbott Molecular Due...

The Issue: 20 kits of CEP 8 SG ASR Probe (list 06J37-018, lot 440023), contained Vysis...

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

Class III — Low RiskOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: INSTAT - Agent Recalled by Integra LifeSciences Corporation Due to Due to...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Elekta, Inc.

Recalled Item: Integrity 1.1. Integrity is the interface and control software for Recalled...

The Issue: The problem is that the "static tolerances" from the calibration files...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Baxter Healthcare Corp.

Recalled Item: A) Product Code 2N8220: Non-DEHP Catheter Extension Set Kit Recalled by...

The Issue: Customers have reported that when separating an individual package from its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Colla Tape Absorbable Collagen Wound Dressing for Dental Surgery The...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: NeuraWrap Nerve Protector NeuraWrap Nerve Protector is indicated for the...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing