Medtronic Icd Recall 2025. A total of 48 devices implanted in patients may contain a manufacturing defect which would. Class i recall includes evera, viva, brava, claria, amplia, compia and visia.
The record is updated if the fda identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Cobalt xt, cobalt, crome icds.
Medtronic Announced A Recall Of All Implantable Cardioverter Defibrillator And Cardiac Resynchronization Therapy Defibrillators Manufactured After Oct.
Cobalt xt, cobalt, crome icds.
The Record Is Updated If The Fda Identifies A Violation And Classifies The Action As A Recall, And It Is Updated For A Final Time When The Recall Is Terminated.
(1) class i, where there is a reasonable chance that a product will cause serious health problems or death;
Medtronic Icd Recall 2025 Images References :
Class I Recall Includes Evera, Viva, Brava, Claria, Amplia, Compia And Visia.
Medtronic provided physicians with comprehensive patient management recommendations in the communication.
The Record Is Updated If The Fda Identifies A Violation And Classifies The Action As A Recall, And It Is Updated For A Final Time When The Recall Is Terminated.
Medtronic announced a recall of all implantable cardioverter defibrillator and cardiac resynchronization therapy defibrillators manufactured after oct.