FDA Device recall Z-1884-2024
Noblus AC Adapter used with the Noblus Ultrasound Imaging System Model : AHM250PS24
- FDA Device
- Class II
- ongoing
- Published 2024-05-29
On 2024-05-29 the FDA classified a Class II recall of Noblus AC Adapter used with the Noblus Ultrasound Imaging System Model : AHM250PS24 by Fujifilm Healthcare Americas, citing 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 t….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1884-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-04-11 |
| Published | 2024-05-29 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Fujifilm Healthcare Americas |
| Distribution | US |
Product
Noblus AC Adapter used with the Noblus Ultrasound Imaging System Model : AHM250PS24
Reason
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).
Identifiers
| code_info | UDI-DI: (01) 04580292771704 Noblus Ultrasound Imaging System AC Adapter Serial Number Before K17160001 (Excluding K17160001) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1884-2024%22
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