FDADecember 12, 2024device

ALTRUA 2 DR Pacemaker, SL (Model Number S702) and EL (Model Number S722)

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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ALTRUA 2 DR Pacemaker, SL (Model Number S702) and EL (Model Number S722) — Recall Details · AllClear