You can find the list of known Avisory here :
Medtronic :
- "Rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glassed) feedthrough, including currently available ICDs and CRT-Ds"
- Reported on June 16 2023
- Devices concerned include the following models:
- DAI Cobalt™ XT/Cobalt™/Crome™ et CRT-D
- Subset of : CRT-D Claria MRI™/Amplia MRI™/Compia MRI™/Viva™/Brava™
- Subset of : DAI Visia AF™/Visia AF MRI™/Evera™/Evera MRI™/Primo MRI™/Mirro MRI™ - For more informations, please check the following link :
Medical device recall - US Food & Drung Administration