Jolife recalls LUCAS 2 and 3 chest compression devices due to missing service records. Affected units have specific model numbers and serials. Contact Jolife for details.
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).
Jolife is recalling certain LUCAS 2 and LUCAS 3 chest compression devices because service records were not properly documented. This could lead to improper device function during emergency cardiac procedures.
The hazard involves chest compression systems where service records were not properly documented. This means the device might not function correctly during emergency cardiac procedures if service was performed without proper documentation.
Healthcare professionals using LUCAS devices for cardiac compressions may be affected. Those with the specific model numbers and serials listed are most at risk.
Check for model number 99576 with specific catalog numbers and UDI-DI codes listed in the recall notice. The affected units have unique serial numbers provided in the record.
Reach out to Jolife directly to confirm if your device is affected and get instructions for next steps.
The recall is due to service records not being properly documented for a subset of chest compression systems, which could affect device function during emergency cardiac procedures.
Check for model number 99576 with specific catalog numbers and UDI-DI codes listed in the recall notice. The affected units have unique serial numbers provided in the record.
Contact Jolife directly to confirm if your device is affected and get instructions for next steps.
We’ve drafted a message you can send Jolife to request your refund or repair — edit it as you like.
Subject: Recall Z-2161-2026 — Jolife Jolife Hello, I own a Jolife that is covered by recall Z-2161-2026 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.
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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.
