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. 1,008 recalls have been distributed to Minnesota in the last 12 months.
Showing 36741–36760 of 52,120 recalls
Recalled Item: Persian Recalled by Kwik Trip Bakery Due to Kwik Trip, Inc. is recalling...
The Issue: Kwik Trip, Inc. is recalling various bakery goods which might be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Filled Long Johns 9999954006 Recalled by Kwik Trip Bakery Due to Kwik Trip,...
The Issue: Kwik Trip, Inc. is recalling various bakery goods which might be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cinnamon Cinnsations Recalled by Kwik Trip Bakery Due to Kwik Trip, Inc. is...
The Issue: Kwik Trip, Inc. is recalling various bakery goods which might be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jelly Bismark 9999954008 Recalled by Kwik Trip Bakery Due to Kwik Trip, Inc....
The Issue: Kwik Trip, Inc. is recalling various bakery goods which might be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KBS Plain Bagel Recalled by Kwik Trip Bakery Due to Kwik Trip, Inc. is...
The Issue: Kwik Trip, Inc. is recalling various bakery goods which might be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ice Nuggets Recalled by Kwik Trip, Inc. Due to Kwik Trip Inc reported a...
The Issue: Kwik Trip Inc reported a plastic fan broke which lead to pieces of plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Super Arrow-Flex Percutaneous Sheath Introducer Sets or CL-07635 Recalled by...
The Issue: Arrow has issued a recall for these products due to potential packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 59 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 34 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRCT MIS CR MOB PLT prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 45 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 17 consists of all product under product code: LPH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 6 INCH BEADED FC 1 prosthesis Recalled by Zimmer Biomet, Inc. Due to...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 36 consists of all product under product code: HSB Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 51 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 28 consists of all product under product code: JDI Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 5 consists of all products under product code HWC Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 18 consists of all product under product code: HWC Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 52 consists of product code: HWC and same usage: Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse Treatment Planning System versions 11 Recalled by Varian Medical...
The Issue: When using PBC 11.0.31 to calculate the dose for a conventional arc field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.