FDASeptember 30, 2022device

EMBLEM S-ICD, Subcutaneous Implantable Defibrillators, Model A209, sterile.

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

The hazard

There is an incorrect manufacturing date/timestamp within the software which causes an inaccurate display of battery capacity.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

00802526548406

Recall history

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

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EMBLEM S-ICD, Subcutaneous Implantable Defibrillators, Model A209, sterile. — Recall Details · AllClear