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Jolife AB FDA Recalls
2 recalls on file across devices, 0 of them Class I and 2 still open. This firm is not matched to a listed company.
Newest first
Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.
| Product |
|---|
| LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 MoClass IIApr 13, 2026Due to a subset of chest compression systems/devices where t |
| LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adultClass IIMay 21, 2025Due to demonstration units of chest compression system being |