FDAJune 3, 2021device

Essentio pacemaker, Models: a) L100 b) L101 c) L110 d) L111 e) L121 f) L131

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

The hazard

Latent release of small amounts of hydrogen within the pacemaker may cause a low voltage capacitor to become electrically compromised over time resulting in accelerated battery depletion of the battery and associated progression of displayed battery depletion indicators.

What to do

FDA enforcement status: Ongoing

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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Essentio pacemaker, Models: a) L100 b) L101 c) L110 d) L111 e) L121 f) L131 — Recall Details · AllClear