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. 2,693 recalls have been distributed to Minnesota in the last 12 months.
Showing 1661–1680 of 29,186 recalls
Recalled Item: Z-800W Infusion System. Intended to provide intravenous infusion of...
The Issue: Unreleased software versions were installed on distributed devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800F Infusion System. Intended to provide intravenous infusion of...
The Issue: Unreleased software versions were installed on distributed devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800WF Infusion System. Intended to provide intravenous infusion of...
The Issue: Unreleased software versions were installed on distributed devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: SmartRelease ESTR (Endoscopic soft tissue release system)...
The Issue: Potential that the blade can unintentionally cut tissue prior to the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer C11137 Recalled by Beckman Coulter,...
The Issue: Analyzer has calibration issues where curves switched from passed to failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Valeda Light Delivery System Product Name: Light Based Recalled...
The Issue: U.S. customers were shipped devices that were configured for the European...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800 Infusion System. Intended to provide intravenous infusion of...
The Issue: Unreleased software versions were installed on distributed devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name:...
The Issue: Electrode placement labels on the Digital Acquisition Box (DAB) were applied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: Soltive...
The Issue: Potential for thermal incident including an unexpected occurrence of smoke,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HardyCHROM CRE Recalled by Hardy Diagnostics Due to Identified lots failed...
The Issue: Identified lots failed incoming quality control testing. Lots exhibited...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro...
The Issue: Potential for thermal incident including an unexpected occurrence of smoke,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Premium...
The Issue: Potential for thermal incident including an unexpected occurrence of smoke,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity 4 Birthing Bed Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential for improper crimps on the signal wires of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PhenoMATRIX Recalled by Copan WASP Due to AI-powered bacterial culture plate...
The Issue: AI-powered bacterial culture plate interpretation and workup software does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: Soltive Reusable...
The Issue: Potential for thermal incident including an unexpected occurrence of smoke,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....
The Issue: All RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G7 iOS Application Recalled by Dexcom, Inc. Due to A bug in the 2.7.0...
The Issue: A bug in the 2.7.0 version of the G7 iOS App can cause the app to enter a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus EVIS EXERA III Duodenovideoscope. Model Number: TJF-Q190V Recalled...
The Issue: Recent post-market surveillance data suggests a possible association of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160333 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160325 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.