Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LUCAS 2 Recalled by Jolife AB Due to Due to demonstration units of chest compression system...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Jolife AB directly.
Affected Products
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.
Quantity: 5 units
Why Was This Recalled?
Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Jolife AB
Jolife AB has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report