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.
Showing 38001–38020 of 52,120 recalls
Recalled Item: Medtronic Achieve Cables Recalled by Medtronic Inc. Due to 64 units of...
The Issue: 64 units of Achieve Electrical Cables were shipped with a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker is recalling various lots of the Trithion MIS Modular Distal Capture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 9 Calibrator Recalled by...
The Issue: The firm is conducting a product correction due to an increase in U90-382 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Due to An...
The Issue: An anomaly was identified with the ARIA for Radiation Oncology software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity PACS-IW with Universal Viewer is a device that Recalled by GE...
The Issue: Inaccurate distance measurements with magnified projection X-ray images.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 2.7MM/3.5MM VA-LCP Medial Distal Humerus Plates 10H/RT/186mm-...
The Issue: The 2.7MM/3.5MM VA-LCP Humerus Plates were found to be labeled incorrectly....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity Universal Viewer Version is a device that displays Recalled...
The Issue: Inaccurate distance measurements with magnified projection X-ray images.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cetirizine HCl 10 mg Tablet Recalled by Perrigo Company PLC Due to Failed...
The Issue: Failed Impurity/Degradations Specifications; impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RHINO 7 3000 Recalled by Tf Supplements Due to Undeclared Desmethyl
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACETAMINOPHEN EXTRA-STRENGTH PAIN RELIEVER tablets Recalled by Medline...
The Issue: Labeling: Label Error on Declared Strength- Bottles containing 500 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUROSEMIDE Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...
The Issue: CGMP Deviations: The active pharmaceutical ingredient (API) intended for use...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUROSEMIDE Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...
The Issue: CGMP Deviations: The active pharmaceutical ingredient (API) intended for use...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 Platinum 3000 Recalled by Tf Supplements Due to Undeclared Desmethyl
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets Recalled by Medline...
The Issue: Labeling: Label Error on Declared Strength- Bottles containing 500 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Actavis...
The Issue: Failed Dissolution Specifications: Low Out-of-Specification results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stryker Radius 5.5 to 3.5 Rod to Red Connector Recalled by Stryker Spine Due...
The Issue: Stryker Spine is recalling Radius Rod to Rod Connector 5.5 to 3.5 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airways Development LLC WaterPAP Positive Airway Pressure Device #WP-7700....
The Issue: Airways Development LLC has received a complaint about a canister leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Hemoglobin A1c_3 Recalled by Siemens Healthcare Diagnostics,...
The Issue: Reagent in these lots may demonstrate an increased occurrence of high %HbA1c...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xanax (alprazolam) tablets Recalled by Pfizer Inc. Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shorts on The Beach Golden Edition by Pink Bikini Recalled by Lucy's Weight...
The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.