FDA Recall: Software to enhance designed to prevent initiation of Safety Mode in an ambulatory setting

Company: Boston Scientific Corporation
Date of Enforcement Report: 10/10/2025
Class: I

PRODUCT

ACCOLADE SR SL (Model L300)

Recall Number:

Z-0079-2026

REASON:

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).

RECALLING FIRM/MANUFACTURER:

Boston Scientific Corporation

VOLUME:

16,077 units

DISTRIBUTION:

Worldwide

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