ClearanceBrief
Recall Z-1522-2021 ยท OSR Pacemaker/Icd/Crt Non-Implanted Components

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

CareLink SmartSync Device Manager (24970A). used to interrogate cardiac implantable electronic devices (CIED).

DateApr 6, 2021
StatusOpen, Classified
ReasonThere is a SmartSync software issue that results in an overestimation in the displayed longevity of these devices during an approximate 6-month window of time before the device triggers its Recommended Replacement Time (RRT).
Root causeSoftware design
ActionBeginning 06-APR-2021, Medtronic notified risk managers and practice managers of the field corrective action notification via 2-day UPS delivery of the consignee letter. Confirmation delivery of the consignee letter will be obtained. Medtronic Field Representatives have been instructed to begin installation of the software update. Outside the United States (OUS), communication began on 06- APR-2021 using locally approved methods. Medtronic Field Representatives will begin installation of the software update as it is available locally. Consignees were advised that Medtronic representatives can
Quantity16,311 devices
DistributionWorldwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.