FDADecember 12, 2024device

ESSENTIO DR Pacemaker, SL (Model Number L101, SL MRI (Model Number L111), EL (Model Number L121), and EL MRI (Model Number L131)

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

The hazard

A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built before September 2018, have an increased potential to initiate Safety Mode during telemetry or other normal, higher-power operations due to latent high battery impedance.

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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