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. 2,621 recalls have been distributed to Minnesota in the last 12 months.
Showing 13181–13200 of 29,186 recalls
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 111" 10 Drop Admin Set w/2 Inj Sites Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Homocysteine-In vitro test for the quantitative determination of total...
The Issue: Homocysteine Reagent, Calibration Failures and Quality Control Recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK Hem-O-Lok AutoEndo5 Recalled by Teleflex Medical Due to Certain clip...
The Issue: Certain clip appliers have an increase in misloading and/or jamming related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK AutoEndo5 Recalled by Teleflex Medical Due to Certain clip appliers...
The Issue: Certain clip appliers have an increase in misloading and/or jamming related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neocis Guidance System Fiducial Array - Product Usage: The Neocis Recalled...
The Issue: The Fiducial Array may mismatch their measurement files resulting in failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis MAXI LD PTA Dilatation Catheter Recalled by Cordis Corporation Due to...
The Issue: Product was manufactured utilizing an expired inner body.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...
The Issue: Device may fail to turn on or unexpectedly attempt to restart, rendering it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft Recalled by Ethicon...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.