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.
Showing 48521–48540 of 52,120 recalls
Recalled Item: Casein - 100% Micellar Casein - Rich Chocolate¿2.02 LBS: Soy Lecithin...
The Issue: Source of casein ingredient not listed as milk, an allergen.Consumers who...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: All Natural Whey - Natural Flavor 1.89 LBS: Whey Protein Concentrate and...
The Issue: Source of whey ingredient not listed as milk, an allergen. Consumers who...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Casein - 100% Micellar Casein - Cookies & Cream¿2.02 LBS: Soy Lecithin...
The Issue: Source of casein ingredient not listed as milk, an allergen.Consumers who...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Massive Muscle Gainer- Weight Gainer¿ Dutch Chocolate¿10 LBS: Whey...
The Issue: Source of whey and casein ingredient not listed as milk, an...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sprouts Farmers Market Whey Protein Vanilla: 1 lbs Recalled by Chemi- Source...
The Issue: Source of whey ingredient not listed as milk, an allergen. Consumers who...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: List No. 14212-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14207-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14211-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14200-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14217-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 MeDS Pump Recalled by Fresenius Medical Care Holdings, Inc. dba Renal...
The Issue: Product is being recalled because the combination of the current 50 mg vial,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14219-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas¿ 4800 system z480 instrument. Integrates fully automated total...
The Issue: In rare instances, channel shifted results have been generated with cobas¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14206-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14210-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14203-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog#...
The Issue: The firm is recalling the specific lot due to lower than expected results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP deviations; After quality review of stability failures in previous...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ROCK-IT MAN capsules Recalled by Consumer Concepts, Inc. Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP deviations; After quality review of stability failures in previous...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.