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Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) Recall 87662

Description: CareLink SmartSync Device Manager - Product Usage: used to treat arrhythmias related to bradycardia. Additionally, CRT-P devices can also provide cardiac resynchronization therapy (CRT) in treatment of heart failure, Model Number 24970A

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) Recall 87662 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1528-2021
Event ID87662
Event DescriptionCareLink SmartSync Device Manager - Product Usage: used to treat arrhythmias related to bradycardia. Additionally, CRT-P devices can also provide cardiac resynchronization therapy (CRT) in treatment of heart failure, Model Number 24970A
Product TypeDevices
DistributionWorldwide distribution.
Quantity16,311 units
Recall ReasonA longevity estimation error may occur in the early years of device life when a unipolar pacing vector is programmed in the right atrial (RA) lead and/or the right ventricular (RV) lead. No other device features or therapies are impacted.
Device Classification20210512
Device Code Infoall codes
Center Classification Date20210504
Recall Initiation Date20210406
Recalling FirmMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Initial Notification Letter
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