FDAMarch 15, 2021device

ENDURITY Pulse Generator REF PM**** SN ********* St. Jude Medical Cardiac Rhythm Assurity and Endurity pacemakers are intended to provide single-chamber or dual-chamber bradycardia pacing.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Due to a manufacturing issue associated with the mixing process of the epoxy used in the manufacture of pacemaker from years 2015 through 2018, the affected devices may malfunction caused by moisture ingress through the device header and feedthrough

What to do

FDA enforcement status: Ongoing

Brands named

st jude medical cardian rhythm management division

UPCs

054147345070420541473450705905414734509763054147345097700541473450959605414734509602

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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