Recall database

Compressor, Cardiac, External recalls

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

Showing 1–3 of 3 recalls

Class IIOngoingZ-2161-2026

Jolife AB recalls LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI co…

Due to a subset of chest compression systems/devices where the service performed on the systems were not appropriately documented (The documents for the service performed to justify the passing results were not include i…

Jolife ABMay 20, 2026

Class IIOngoingZ-1998-2025

Jolife AB recalls LUCAS 2

Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.

Jolife ABJul 2, 2025

Class IOngoingZ-1533-2025

ZOLL Circulation, Inc. recalls Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform M…

AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.

ZOLL Circulation, Inc.CAApr 23, 2025