Jolife AB recalls

Jolife AB has 2 recalls on record with the FDA and USDA, the earliest in 2025 and the latest reported on 20 May 2026. 2 are still ongoing. 1 was reported in the last 12 months.

Total recalls2since 2025

Last 12 months1reported

Class I00% of total

Ongoing2latest 20 May 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 1Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 1 0 0Jul 0 0

Severity split

Class I 0 0%Class II 2 100%Class III 0 0%

Why jolife ab is recalled

Other Reasons2100%

Product types

Other Medical Devices2100%

By year

2026150%
2025150%

Ongoing jolife ab recalls

2 active

Reported	Class	Recall	Company	Reason	Where
20 May 2026Device	CLASS II	Lucas 2 Model Number: 99576 Catalog Numbers recalled by Jolife AB	Jolife AB	Other	Nationwide
2 Jul 2025Device	CLASS II	Lucas 2, 3 and 1 Lucas chest compression System is to be recalled	Jolife AB	Other	Nationwide

All jolife ab recalls, newest first

2 total

Reported	Class	Recall	Company	Reason	Where
20 May 2026Device	CLASS II	Lucas 2 Model Number: 99576 Catalog Numbers recalled by Jolife AB	Jolife AB	Other	Nationwide
2 Jul 2025Device	CLASS II	Lucas 2, 3 and 1 Lucas chest compression System is to be recalled	Jolife AB	Other	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.