FDAMay 21, 2025device
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.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.
What to do
FDA enforcement status: Ongoing
Brands named
jolife abjolife
UPCs
995760000250088387390456521331000081008838738618759457600000500883873834329
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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