# FDA recall Z-3030-2026

> **FUJIFILM Healthcare Americas Corporation** · Class II · device recall initiated 2026-07-22.

## Product

FUJIFILM Synapse PACS software v7.4.310; radiological  image processing system

## Reason for recall

Software issue may cause the ruler measurement to be inaccurate.

## Distribution

Worldwide - US Nationwide distribution in the states of NY, VA, KS, OR, OH, and the country of Australia.

## Key facts

- **Recall number:** Z-3030-2026
- **Recalling firm:** FUJIFILM Healthcare Americas Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-22
- **Report date:** 2026-09-02

- **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-3030-2026

## Citation

> MORVS. FDA recall Z-3030-2026. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-3030-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*