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Jolife AB

3 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00 recall (Z-2161-2026)Jolife AB2026-05-11
LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external ca recall (Z-1998-2025)Jolife AB2025-06-20
LUCAS 2 Chest Compression System. The device's Instruction for Use is labeled in part: "LU recall (Z-1664-2011)Jolife AB2011-03-16

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