FDAJuly 11, 2023device

EMBLEM S-ICD Pulse Generator Model A209; Subcutaneous Implantable Cardioverter Defibrillator

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

The hazard

There is a potential for a rare interaction between the EMBLEM S-ICD and LATITUDE communicator, which may cause S-ICD sensing disablement for a 24-hour interval.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

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Recall history

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

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