---
title: "Jolife AB Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search Jolife AB recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/jolife-ab/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# Jolife AB recall records

**2** reported ongoing

2 records in this archive. Latest source date Apr 13, 2026.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## Records and reported status

Apr 13, 2026 FDA device enforcement

### [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: 0088...](https://isitonrecall.com/recall/fda-device-z-2161-2026-lucas-2-model-number-99576-catalog-numbers-99576-000024-and-99576-000011-udi-di-code-00883873904565/)

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).

Class II Reported ongoing

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.

[Official source for LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 008838739...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2161-2026%22)

May 21, 2025 FDA device enforcement

### [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 absen...](https://isitonrecall.com/recall/fda-device-z-1998-2025-lucas-2-3-and-3-1-lucas-chest-compression-system-is-to-be-used-for-performing-external-cardiac-compr/)

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

Class II Reported ongoing

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

[Official source for LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac c...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1998-2025%22)

## Reasons in these listed records

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

These examples come from this result page and are not a ranking of every recall reason.

## Checking Jolife AB

### Is there a recall on jolife ab right now?

This archive contains 2 records, including 2 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

[Search Jolife AB](https://isitonrecall.com/check/?q=Jolife%20AB) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
