FUJIFILM Healthcare recalls Noblus AC adapters for ultrasound systems that may overheat and cause smoke if power cables are frequently plugged in and out.
AC adapters of Noblus can heat up, and cause smoke in the worst case, when an excessive mechanical stress is applied to the socket for power cable (frequent insertion/removal of the power cable).
FUJIFILM Healthcare is recalling Noblus AC adapters used with the Noblus Ultrasound Imaging System Model AHM250PS24. The adapters can heat up and cause smoke if the power cable is frequently inserted or removed, which could lead to fire or injury.
The AC adapters can overheat and produce smoke when the power cable is subjected to frequent insertion or removal. This mechanical stress can cause the adapter to fail, potentially leading to fire or injury.
Users of the Noblus Ultrasound Imaging System Model AHM250PS24 with the specified AC adapters are affected. Medical professionals using these systems are most at risk due to potential fire or injury from overheating.
Check for the Noblus Ultrasound Imaging System Model AHM250PS24 with AC adapters having a serial number before K17160001 (excluding K17160001). The UDI-DI number is (01) 04580292771704.
Look for the serial number on the adapter, which should be before K17160001 (excluding K17160001).
No, this recall is specific to the Noblus Ultrasound Imaging System Model AHM250PS24 with the affected AC adapters.
Check the adapter's serial number, which should be before K17160001 (excluding K17160001), and the UDI-DI number (01) 04580292771704.
The recall record does not specify a remedy, so contact FUJIFILM Healthcare for further instructions.
We’ve drafted a message you can send FUJIFILM Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1884-2024 — FUJIFILM Healthcare FUJIFILM Healthcare Hello, I own a FUJIFILM Healthcare that is covered by recall Z-1884-2024 from FUJIFILM Healthcare. 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.
