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. 2,622 recalls have been distributed to Minnesota in the last 12 months.
Showing 12341–12360 of 29,186 recalls
Recalled Item: TEG Manager software versions used in conjunction with TEG 5000 are 1.1.0...
The Issue: Software defect in TEG Manager impacts the displayed alert for out of range...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Enterococcus faecalis derived from ATCC 51299 In Vitro Diagnostic...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to Tests returning incorrect...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Firefly Floorsitter Recalled by James Leckey Design Ltd Due to The firm...
The Issue: The firm received reports of a number of broken latches on the floorsitter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chemistry QC Premium Plus Recalled by Randox Laboratories Ltd. Due to The...
The Issue: The control target and range value for Sodium using the ISE indirect method...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB HiResolution Bionic Ear System Recalled by Advanced Bionics, LLC Due to...
The Issue: hearing performance degradation due to body-fluid entering the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB HiResolution Bionic Ear System Recalled by Advanced Bionics, LLC Due to...
The Issue: hearing performance degradation due to body-fluid entering the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Cogent Hemodynamic Monitoring System. Recalled by ICU Medical, Inc. Due...
The Issue: Firm identified software issues which leads to the patient ID and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ev3 Pipeline Flex Embolization Device. For neurological endovascular use....
The Issue: Embolization device delivery system may fracture at the distal section...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Ethyl Alcohol Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The assay may exhibit a positive bias in QC and patient results within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS....
The Issue: Embolization device delivery system may fracture at the distal section...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software issue could potentially cause the stand and table movements to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software issue could potentially cause the stand and table movements to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software issue could potentially cause the stand and table movements to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DFINE Vertebral Assemblies: Hydraulic-Master Syringe Assembly Recalled by...
The Issue: Vertebral hydraulic assemblies has incorrect expiration date printed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DFINE Vertebral Hydraulic Assemblies: Hydraulic Assembly Recalled by Merit...
The Issue: Vertebral hydraulic assemblies has incorrect expiration date printed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE MAGEC 2 Rod X.X mm XX mm Recalled by NuVasive Inc Due to...
The Issue: Post-implantation separation of an actuator end cap component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.