Class II

Medical Device Recall: 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 br

Jolife AB · May 21, 2025

Reason for Recall

Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.

Product Description

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.

Distribution

U.S. Nationwide distribution in the states of IN, MI, OH and TX.

States Affected

NATIONWIDE

Quantity Affected

5 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1998-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Jolife AB Medical Device Recall: 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 br | SafeCheck