Class IIOngoingZ-0773-2025
Medtronic Neuromodulation recalls SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG…
Software issues were identified in application version 2.x.
Medtronic Neuromodulat…MNJan 8, 2025
Recalls in Minnesota
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 229–233 of 233 recalls
Class IIOngoingZ-0772-2025
Medtronic Neuromodulation recalls SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG…
Software issues were identified in application version 2.x.
Medtronic Neuromodulat…MNJan 8, 2025
Class IIOngoingZ-0771-2025
Medtronic Neuromodulation recalls SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG…
Software issues were identified in application version 2.x.
Medtronic Neuromodulat…MNJan 8, 2025
Class IIOngoingZ-0743-2025
3M Company - Health Care Business recalls Clarity Precision Grip Attachments
Attachments may not mate with the tooth as intended in the digital treatment design.
3M Company - Health Ca…MNJan 1, 2025
Class IIOngoingZ-0727-2025
Beckman Coulter, Inc. recalls Access hsTnI Reagent
Beckman Coulter, Inc. is recalling their Access hsTnI assay, a medical device by correction. The reason for the recall is: high troponin antigen (>55,000 pg/mL) can contaminate an analyzers probe and cause inter-assay ca…
Beckman Coulter, Inc.MNJan 1, 2025