FDANovember 13, 2020device

EMBLEM S-ICD Subcutaneous Electrode Model 3501. Component of implantable cardioverter defibrillator (ICD)

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

The hazard

There is potential for fractures which results in the inability to delivery therapy.

What to do

FDA enforcement status: Terminated

Brands named

boston scientificboston

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 Electrode Model 3501. Component of implantable cardioverter defibrillator (ICD) — Recall Details · AllClear