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. 2,439 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,439 in last 12 months

Showing 3726137280 of 52,120 recalls

Medical DeviceDecember 2, 2015· Gsi Group Inc

Recalled Item: PRN 50-M+ Recalled by Gsi Group Inc Due to The item was recalled due to an...

The Issue: The item was recalled due to an increased user/patient risk of exposure to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Best Practice Kits containing certain production lots of Endo GIA Recalled...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Biomet, Inc.

Recalled Item: Green Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a...

The Issue: There may be a separation and an insufficient weld between the spring and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Biomet, Inc.

Recalled Item: Black Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a...

The Issue: There may be a separation and an insufficient weld between the spring and...

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

Class II — Potential Health HazardOngoing
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Coconut Cardamom - Sprouted Almond Spread. Product is packaged in glass jars...

The Issue: Coconut Cardamom- Sprouted Almond Spread is recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Hazelnut Raw Cacao - Sprouted Hazelnut Spread. Product is packaged in glass...

The Issue: Hazelnut Raw Cacao - Sprouted Hazelnut Spread is recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Cashew Cardamom - Sprouted Cashew Almond Spread. Product is packaged...

The Issue: Cashew Cardamom - Sprouted Cashew Almond Spread is recalled because it has...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Superberry Maqui Camu - Sprouted Almond Spread. Product is packaged Recalled...

The Issue: Superberry Maqui Camu - Sprouted Almond Spread is recalled because it has...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Cinnamon Red Maca - Sprouted Almond Spread. Product is packaged in glass...

The Issue: Cinnamon Red Maca - Sprouted Almond Spread is recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 2, 2015· Pfizer Inc.

Recalled Item: Norpace CR (disopyramide phosphate) extended-release capsules USP Recalled...

The Issue: Failed Dissolution Specification

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 23 Recalled by Beckman Coulter...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 34 Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· 3M Company - Health Care Business

Recalled Item: 3M Coban Self-Adherent Wrap Shipper carton label identified the product...

The Issue: Product mislabeled as latex free. Actual Catalog number 1581, lot 2020-10AN....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· JosNoe Medical, Inc.

Recalled Item: PS-500 Scope Warmer Recalled by JosNoe Medical, Inc. Due to Damage to...

The Issue: Damage to package seals potentially compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 20 Recalled by Beckman Coulter...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 33 Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing