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. 2,494 recalls have been distributed to Minnesota in the last 12 months.
Showing 23121–23140 of 52,120 recalls
Recalled Item: Losartan Potassium Tablets USP 25 mg 1000 count bottle NDC Recalled by...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP 100 mg 1000 count bottle NDC Recalled by...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP 100 mg 90 count bottle NDC Recalled by Golden...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP 25 mg 90 count bottle NDC Recalled by Golden...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Recalled by...
The Issue: Mixer blade may separate from mixer due to the screw and nut failure and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 0-arm TM 1000 Imaging Systems: Bl-700-00027-XXX and...
The Issue: The 0-arm 1000 Imaging System uses energy from the batteries to generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott MitraClip XTR Clip Delivery System Recalled by Abbott Vascular Due to...
The Issue: Reports of implantable mitral valve repair system clips unexpectedly opening...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Sagent Pharmaceuticals Inc Due...
The Issue: Lack of Sterility Assurance: Microbial growth detected during a routine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mycophenolate Mofetil for Injection Recalled by Par Pharmaceutical, Inc. Due...
The Issue: Presence of Particulate Matter; glass fragment observed in one vial of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Item code: 8881200029 Recalled by...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.