Jolife AB
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-05-20 to 2026-05-20
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-05-20 | FDA Device | FDA Recall: LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 008838739 | Jolife AB | Class II | N/A |