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. 2,489 recalls have been distributed to Minnesota in the last 12 months.
Showing 24021–24040 of 52,120 recalls
Recalled Item: Alere Cholestech LDX Analyzer Recalled by Alere San Diego, Inc. Due to The...
The Issue: The polarity of the output of power supply was reversed. Due to polarity of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Force TriVerse electrosurgical device 10 cord-Intended as...
The Issue: Potential for the sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane...
The Issue: Complaints received that products packaged with the incorrect introducer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS with Option syngo DE Scan for Single Recalled by...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Edge Plus Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...
The Issue: The devices were released from a lot for which one sample failed to meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...
The Issue: The devices were released from a lot for which one sample failed to meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ciclopirox shampoo 1% Recalled by Perrigo New York, Inc. Due to Failed...
The Issue: Failed Degradation/Impurities Specifications: Out of specification related...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lovastatin Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: Finished product made with lovastatin drug substance that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Big Daddy s Bold Cheese Pizza Recalled by Schwan's Global Supply Chain,...
The Issue: Cheese pizza may contain plastic pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nature's Nectar High Pulp Orange Juice Recalled by Citrus Systems Inc Due to...
The Issue: Product cannot be verified as having achieved a 5-log reduction per 21 CFR 120.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Discovery Ml DR Product Usage: The systems are intended for Recalled by GE...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery Ml Product Usage: The systems are intended for head Recalled by GE...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery PET/CT 610 Product Usage: The systems are intended for Recalled by...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima PET/CT 560 Recalled by GE Healthcare, LLC Due to GE Healthcare PET/CT...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery PET/CT 710 Product Usage: The systems are intended for Recalled by...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery IQ Product Usage: The systems are intended for head Recalled by GE...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula Recalled...
The Issue: Packaged with an incorrect size inner cannula.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.