# FDA recall Z-1884-2024

> **FUJIFILM Healthcare Americas Corporation** · Class II · device recall initiated 2024-04-11.

## 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).

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1884-2024
- **Recalling firm:** FUJIFILM Healthcare Americas Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-11
- **Report date:** 2024-05-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lexington, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1884-2024

## Citation

> AI Analytics. FDA recall Z-1884-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1884-2024. Source: US FDA. Licensed CC0.

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