FDADecember 12, 2024device

ACCOLADE DR Pacemaker, SL (Model Number L301), SL MRI (Model Number L311), EL (Model Number L321), and EL MRI (Model Number L331)

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

0080252655917400802526559181

Recall history

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

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