Jolife recalls LUCAS 2, 3, and 3.1 chest compression systems for potential clinical use. This could lead to unsafe medical procedures if used outside intended purposes.
Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.
Jolife is recalling LUCAS 2, 3, and 3.1 chest compression systems because they may be used for clinical purposes without proper authorization. This poses a risk of unsafe medical procedures if the devices are used outside their intended purpose.
The hazard arises because the devices were provided to customers for clinical use without proper authorization. This could lead to unsafe medical procedures if the systems are used outside their intended purpose.
Users of the LUCAS chest compression systems who may have them for medical purposes are affected. Healthcare professionals or individuals with medical training are at higher risk.
Check for LUCAS 2, 3, or 3.1 models with specific catalog numbers and serial numbers listed in the recall notice. The devices are intended for external cardiac compressions on adult patients with acute circulatory arrest.
Identify the model and serial number to confirm if your device is recalled.
The recall is due to demonstration units being provided to customers for potential clinical use without proper authorization.
LUCAS 2, 3, and 3.1 models with specific catalog numbers and serial numbers listed in the recall notice.
The recall record does not specify a remedy.
We’ve drafted a message you can send Jolife to request your refund or repair — edit it as you like.
Subject: Recall Z-1998-2025 — Jolife Jolife Hello, I own a Jolife that is covered by recall Z-1998-2025 from Jolife. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.