FDAMarch 10, 2022device

Merlin PCS 3650 programmer Model 3330 software

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

The hazard

Due to a programmer software anomaly under very specific circumstance when executing a pacing capture Decrement Test in-clinic on implantable cardioverter and cardiac resynchronization therapy defibrillator devices, the programmer may continue to execute the Decrement Test instead of terminating the test and restoring the permanent programmed pacing parameters.

What to do

FDA enforcement status: Ongoing

Brands named

st jude medical cardiac rhythm management division

UPCs

05414734509725

Recall history

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

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