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All product recalls associated with Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF).
Total Recalls
156
Past Year
0
Class I (Serious)
0
Most Recent
May 2023
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The firm's internal processes identified that certain lots may have an improperly sealed barrier that could potentially compromise sterility.
Telemetry error that may occur with Medtronic Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds).
Telemetry error that may occur with Medtronic Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds).