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 25321–25340 of 52,120 recalls
Recalled Item: APTIO RACK INPUT MODULE Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLAB CORE UNIT / LYNX WITH IOM Recalled by Siemens Healthcare...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO INPUT/OUTPUT MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLAB - STORAGE MODULE 9000 Recalled by Siemens Healthcare Diagnostics,...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLAB - STORAGE MODULE 15000 Recalled by Siemens Healthcare Diagnostics,...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO RACK OUTPUT MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO 9000 STORAGE MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO CENTRIFUGE MODULE Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portable Suction Pump Recalled by Ohio Medical Corporation Due to The...
The Issue: The care-e-vac(R)3 Battery/AC Powered Portable Aspirator battery terminal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVS Aria Cage Recalled by Stryker Spine Due to The anterior and posterior...
The Issue: The anterior and posterior markers on the cage were on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK(R) 2 AST-P655 Recalled by bioMerieux, Inc. Due to Routine internal...
The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK(R) 2 AST-P640 Recalled by bioMerieux, Inc. Due to Routine internal...
The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IsoFlex LAL Support Surface Recalled by Stryker Medical Division of Stryker...
The Issue: Certain 2860 IsoFlex LAL support surfaces were assembled with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kit For...
The Issue: A deterioration of performance was identified with influenza type B Enzyme...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyclosporine 1% Human Eye Drops Recalled by Westlab Pharmacy, Inc. dba...
The Issue: Lack of Process Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADAA Cataract Drops Recalled by Westlab Pharmacy, Inc. dba Westlab Pharmacy...
The Issue: Lack of Process Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprostadil 500 mcg/mL Injectable Recalled by Westlab Pharmacy, Inc. dba...
The Issue: Incorrect Product Formulation
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pointe Scientific AutoHDL/LDL Cholesterol Calibrator Recalled by Medtest...
The Issue: Vials of the autoHDL/LDL Calibrator were shipped without a vial label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contrave (naltrexone HCl and bupropion HCl) Extended-Release Tablets...
The Issue: Defective Container: Customer complaints of punctures in the bottle.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ambu Aura40 Standard Recalled by Besmed Health Business Corporation Due to...
The Issue: Ambu Aura40 Standard, Reusable Laryngeal Mask packaged in a pouch marked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.