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FDA (Device enforcement)Recalled 2025-05-21class ii

Jolife AB: 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 sponta

Hazard

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

Details from the source

Reason for recall: Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use. Distribution: U.S. Nationwide distribution in the states of IN, MI, OH and TX. Quantity: 5 units Lot/code info: Lucus 2 Catalog Number: 99576-000025 UDI-DI code: 00883873904565 Serial Number: 30090111 Lucas 3 Catalog Number: 21331-000081 UDI-DI code: 00883873861875 Serial Numbers: 35172335 35160570 Lucas 3.1 Catalog Number: 94576-000005 UDI-DI code: 00883873834329 Serial Numbers: 3518A164 3518D104 (Scrapped)

UPC codes

00883873904565, 00883873861875, 00883873834329

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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