# FDA recall Z-2161-2026

> **Jolife AB** · Class II · device recall initiated 2026-04-13.

## Product

LUCAS 2  Model Number: 99576  Catalog Numbers: 99576-000024 and 99576-000011  UDI-DI code: 00883873904565    LUCAS 3  Model Number: 99576  Catalog Number: 99576-000043  UDI-DI code: 00883873861875    LUCAS 3.1  Model Number: 99576  Catalog Number: 99576-000063  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.

## Reason for recall

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).

## Distribution

U.S. Nationwide distribution in the states of AL, AZ, CA, FL, HI, IA, KS, KY, LA, MA, MD, MN, NC, NV, OH, SC, TX, UT, VA, WA, and WY.

## Key facts

- **Recall number:** Z-2161-2026
- **Recalling firm:** Jolife AB
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-13
- **Report date:** 2026-05-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lund, Sweden

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2161-2026

## Citation

> MORVS. FDA recall Z-2161-2026. Retrieved 2026-10-20 from https://api.morvs.ai/recall/Z-2161-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*