Jolife AB recalls
2 official recalls and safety alerts involving Jolife AB since 2025-07, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Jolife AB or the relevant agency.
- 2026-05-20
USJolife AB recalls LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Number: 99576 Catalog…
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…
FDA · DeviceJolife ABU.S. Nationwide distribution in the states of AL, AZ, CA, FL, HI, IA, KS, KY,…Official notice →- 2025-07-02
- US
Jolife AB recalls LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have…
Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.
FDA · DeviceJolife ABU.S. Nationwide distribution in the states of IN, MI, OH and TX.Official notice →