FDAAugust 20, 2025device

Model Number L209 PROPONENT DR (VDD) SL Pacemaker

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

The hazard

Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps).

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

0080252655906800802526576386

Recall history

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

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Model Number L209 PROPONENT DR (VDD) SL Pacemaker — Recall Details · AllClear