Reported May 20, 2026 · Ongoing
LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model…
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?
3 of 3 products
| Model / number | Barcodes | Product as published |
|---|---|---|
99576 | 00883873904565 | Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 |
99576-000043 | 00883873861875 | Model Number: 99576 UDI-DI code: 00883873861875 LUCAS 3.1 |
99576-000063 | 00883873834329 | Model Number: 99576 UDI-DI code: 00883873834329 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
- LUCAS 2 Model Number99576
- Catalog Numbers99576-000024
- and 99576-000011 UDI-DI code00883873904565
- Serial Numbers
301008463011212530123845301243483012444030124475301249913013660530148155301483653015B5683015B6823015C2763015C7223015C7233015C7243015F2463015F5873016G8453016H9833017K0783017K0793017K080
- LUCAS 3 Model Number99576
- Catalog Number99576-000043
- UDI-DI code00883873861875
- Serial NumbersLUCAS 3.1
35160778351732723517346135185820351858173517504035175039351733473516092135175373351742793517270135161449
- Model Number99576
- Catalog Number99576-000063
- UDI-DI code00883873834329
- Serial Numbers
117 of 117 codes
3520R7633522AN953519F6153520N4193522DK483521S5743521T9013520R1873518B3003522EG063520P7493520R2063520S0053520P5123520P6913520P7413520P7423520P7443520P7453520P7463520P7483520P8103520S0063520P7473520S0033521AF213518B1313520L4083519E7433521AC183521U3793520O3643520S2923519F0353520S1493521Z4953521Z4963520P0823520L9573520R1803519G2353519G6333519H5683519E6073522BI323518D0283522CN473520K8673519I4253520K9233523FA453520O7713520R1233521W0203520K9663522AV783521T5683520O7763518A7073521T325
- Amount recalled
- 153 systems
Where it was sold
Why it was recalled
Due to a subset of chest compression systems/devices where the service performed on the systems were not appropriately documented (The documents for the service performed to justify the passing results were not include in the service records).
This product could cause temporary or reversible health problems — stop using it.
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