Reported Jul 2, 2025 · Ongoing
LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult…
Jolife AB
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Jolife AB · Scheelevagen 17 · Lund · N/A
Is this the product you have?
- 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.
- Lot codes and dates
- Lucus 2 Catalog Number99576-000025
- UDI-DI code00883873904565
- Serial Number30090111
- Lucas 3 Catalog Number21331-000081
- UDI-DI code00883873861875
- Serial Numbers35172335 35160570 Lucas 3.1
- Catalog Number94576-000005
- UDI-DI code00883873834329
- Serial Numbers3518A164 3518D104 (Scrapped)
- Amount recalled
- 5 units
Where it was sold
Why it was recalled
Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.
This product could cause temporary or reversible health problems — stop using it.
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