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. 2,400 recalls have been distributed to Minnesota in the last 12 months.
Showing 42801–42820 of 52,120 recalls
Recalled Item: Human Subclass Kit for use on the Beckman IMMAGE"/IMMAGE"800 Analyser...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human lgG4 Subclass kit for use on the Beckman Coulter Recalled by The...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human lgG4 Subclass Liquid Reagent Kits Human lgG1& lgG2 Antisera Recalled...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MininephThl Human lgG4 Kit Product Code: ZK009.LR This kit is Recalled by...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human lgG4 Subclass Liquid Reagent Kits For use on the Recalled by The...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human lgG4 Subclass Liquid Reagent Kits for use on the Recalled by The...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human lgG Subclass Liquid Reagent Kits for use on the Recalled by The...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 Recalled by Abbott...
The Issue: 17% of ARCHITECT Total T3 Reagent Kit, LN 7K64-20/-25 reagent lots 38901UI00...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASSEMBLY Recalled by Intuitive Surgical, Inc. Due to Correction due to the...
The Issue: Correction due to the detection of a motor sensor failure in the Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frozen beer battered onion rings packaged in 40 oz plastic bags Recalled by...
The Issue: Product may be contaminated with glass.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frozen battered onion rings packaged in 40 oz plastic bags Recalled by...
The Issue: Product may be contaminated with glass.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Buprenorphine Hydrochloride Injection Recalled by Hospira Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specification: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Persona The Personalized Knee System 2.5 mm Female Screw 48 Recalled by...
The Issue: The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Potassium Chloride Injection Recalled by Baxter Healthcare Corp Due to...
The Issue: Correct Labeled Product Mispack: Shipping cartons labeled as containing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xoran MiniCAT X-ray imaging device Recalled by Xoran Technologies, LLC Due...
The Issue: Out of tolerance kVp, Unexposed (black) frames, and Out of tolerance Dose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D'errico perforator drills are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A zipser clamp is an instrument used to compress reduce Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKenzie enlarging burrs are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gardner-Wells traction tongs are skull tongs for traction used to Recalled...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson cranial drill sets (w/ brace and 5 attachments) are Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.