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. 2,673 recalls have been distributed to Minnesota in the last 12 months.
Showing 5041–5060 of 29,186 recalls
Recalled Item: ENDOPATH ECHELON 45mm RELOADS WITH GRIPPING SURFACE TECHNOLOGY (GST)...
The Issue: There is the potential for incomplete staple line formation during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Distal Cover MAJ-2315 Used with: EVIS EXERA III Recalled by...
The Issue: Single Use Distal Cover MAJ-2315 may unexpectedly detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Recalled by...
The Issue: Loss of connectivity between the FlexArm and the Table due to a software issue.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Recalled by...
The Issue: Loss of connectivity between the FlexArm and the Table due to a software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code 0848 Recalled by Megadyne Medical Products, Inc. Due to...
The Issue: Affected product codes are now limited to use in patients age 12 years or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code 0847 Recalled by Megadyne Medical Products, Inc. Due to...
The Issue: Affected product codes are now limited to use in patients age 12 years or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code 0846 Recalled by Megadyne Medical Products, Inc. Due to...
The Issue: Affected product codes are now limited to use in patients age 12 years or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code 0845 Recalled by Megadyne Medical Products, Inc. Due to...
The Issue: Affected product codes are now limited to use in patients age 12 years or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terragene Bionova PCD (PCD222-C) Recalled by TERRAGENE S.A. Due to Due to a...
The Issue: Due to a discrepancy between the FDA-Cleared Indications for Use (IFU) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terragene Integron IT26-C Terragene Integron IT26-C with extender Benco...
The Issue: Due to a discrepancy between the FDA-Cleared Indications for Use (IFU) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt XT DR MRI SureScan Implantable Cardioverter Defibrillator Recalled by...
The Issue: During internal review of Polaris battery assembly data from the HiPot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker, Inc. Due to The microcatheter IFU...
The Issue: The microcatheter IFU contains an intended use that has not been evaluated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker, Inc. Due to The microcatheter IFU...
The Issue: The microcatheter IFU contains an intended use that has not been evaluated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accure Laser System Recalled by Accure Acne, Inc Due to Laser system's spot...
The Issue: Laser system's spot tracking system may become misaligned resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Flo-Thru Intraluminal Shunt Recalled by Baxter Healthcare Corporation...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Floseal Hemostatic Matrix Fast Prep Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascu-Guard Peripheral Vascular Patch (US) Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter FloSeal Hemostatic Matrix NL Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Flo-Rester Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERI-GUARD SUPPLE Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.