Jolife AB: Medical Device Recall in 2025 - (Recall #: Z-1998-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: May 21, 2025

Date Posted: July 2, 2025

Recall Number: Z-1998-2025

Event ID: 96729

Reason for Recall:

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

Status: Ongoing

Product Quantity: 5 units

Code Information:

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)

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated