Jolife Ab recalls

Jolife Ab appears in 2 official U.S. recall notices indexed by RecallRadar, most recently on 2026-05-20.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Number: 99576 Catalog…
  FDA Device · Class II · 2026-05-20 · Jolife Ab
• LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acu…
  FDA Device · Class II · 2025-07-02 · Jolife Ab