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Jolife AB recalls LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult
Recalled July 2, 2025 · FDA recall Z-1998-2025 · Jolife AB
Hazard
Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use. · FDA Class II
Units
5 units
Sold at
U.S. Nationwide distribution in the states of IN, MI, OH and TX.
Description
Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.
Product
LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.
Manufacturer(s)
Jolife AB
Made in
Sweden
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →