Class II

Medical Device Recall: FUJIFILM Synapse PACS software v7.4.310; radiological image processing system

FUJIFILM Healthcare Americas Corporation · July 22, 2026

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.

States Affected

NATIONWIDE

Quantity Affected

6 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3030-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.