Jolife AB Recalls
2 recalls on record · July 2, 2025 to May 20, 2026 · Medical Devices
Recalls by year
25
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 20, 2026Medical DevicesFDA
Jolife AB recalls LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Mo
Hazard: 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 in the service records).
July 2, 2025Medical DevicesFDA
Jolife AB recalls LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult
Hazard: Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.