FDAMarch 15, 2021device

ASSURITY Pulse Generator REF PM**** SN ********* ST. JUDE MEDICAL 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

0541473450706605414734507073054147345070970541473450957205414734509589

Recall history

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

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