Recall database

HeartSine Technologies Ltd recalls

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

Showing 1–2 of 2 recalls

Class IIOngoingZ-0288-2026

Due to customer complaints, defibrillator pads may contain damage pins that disrupt the mechanical fit and electrical contact.

HeartSine Technologies…Oct 29, 2025

Class IIOngoingZ-2174-2025

Due to a component manufacturing issue, Automated External Defibrillator may not function properly (deliver shocks)

HeartSine Technologies…Aug 6, 2025