fda_recall · device_recall · high

Jolife AB — Class II recall: LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UD…

Event date
2026-05-20 00:00:00Z
Observed
2026-07-09 22:52:33Z
Source ID
Z-2161-2026
Payload hash
6375b444057c8bf3e74c8185

Summary

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). Status: Ongoing.

Entities

Informational only. Not legal, financial, or medical advice.