Noblus AC Adapter used with the Noblus Ultrasound Imaging System… — Class II medical device recall Z-1884-2024
Ongoing recall by FUJIFILM Healthcare Americas Corporation, reported 2024-05-29, distributed nationwide. AC adapters of Noblus can heat up, and cause smoke in the worst case, when an excessive mechanical stress is a
| Recall number | Z-1884-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | FUJIFILM Healthcare Americas Corporation, Lexington, MA, United States |
| Recall initiated | 2024-04-11 |
| Classified | 2024-05-22 |
| Reported by FDA | 2024-05-29 |
| Distributed | Nationwide (US) |
| Quantity | 418 units |
| UPC / GTIN / UDI-DI | 04580292771704 |
| Model numbers | AHM250PS24 |
Product
Noblus AC Adapter used with the Noblus Ultrasound Imaging System Model : AHM250PS24
Reason for recall
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).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1884-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.