Recall database

Implantable Pulse Generator, Pacemaker (Non-Crt) recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 25–26 of 26 recalls

Class IOngoingZ-0823-2025

Boston Scientific Corporation recalls PROPONENT DR Pacemaker

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 lat…

Pacemaker (Non-Crt) Implantable Pulse Generator
Process design

Boston Scientific Corp…MNJan 22, 2025

Class IOngoingZ-0822-2025

Boston Scientific Corporation recalls ACCOLADE DR Pacemaker

Pacemaker (Non-Crt) Implantable Pulse Generator
Process design

Boston Scientific Corp…MNJan 22, 2025