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. 2,505 recalls have been distributed to Minnesota in the last 12 months.
Showing 21861–21880 of 29,186 recalls
Recalled Item: Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW...
The Issue: Due to the potential for reporting erroneous results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is voluntarily recalling its Chariot" Guiding Sheath. To...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 - Foam of 100 tests WW. Recalled by Biomerieux...
The Issue: Due to the potential for reporting erroneous results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 - Foam of 100 tests US. Recalled by Biomerieux...
The Issue: Due to the potential for reporting erroneous results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Radiation therapy system Recalled by Mevion Medical Systems,...
The Issue: The treatment table positioning belt can slip gear positions, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressit-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...
The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software version VD10E for Syngo X-Workplace Recalled by Siemens Medical...
The Issue: Potential post-processing software issue when using tabcard "4D" on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCM CombiM Modules 903-111 Recalled by Radiometer America Inc Due to...
The Issue: Radiometer America, Inc. is recalling TCM CombiM on rare occasions they may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressol-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...
The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Integral Centralizer Hip System Recalled by Biomet, Inc. Due to PMMA...
The Issue: PMMA is listed as a material on the label but the product does not contain PMMA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Recalled by...
The Issue: Lumenis Ltd Announces a Field Action of the M22 IPL Acne Filters for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet is initiating a...
The Issue: Zimmer Biomet is initiating a recall of the Virage Occipital Eyelet, as it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus ENDOEYE HD II Video Telescopes. Models WA50040A ENDOEYE HD II...
The Issue: A damaged temperature sensor at the ENDOEYE tip caused the distal end to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer K2 EDTA (K2E) 5.4mg Plus Blood Collection Tubes. Recalled by...
The Issue: Some tubes were manufactured with the stopper not fully inserted into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERMO FISHER 6 DRUG CASSETTE Recalled by Ameditech Inc Due to Ameditechs...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPACS Diagnostic Viewer versions 8.3.7 Recalled by Novarad Corporation...
The Issue: The SUV values that are being calculated in the PET/CT fusion tool are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immutest 10 Pnl Drug Screen Cup w/ Adult Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.