FDA Class II · Medical device · September 2, 2026
FUJIFILM Synapse PACS software v7 recall — FUJIFILM Healthcare Americas Corporation
Software issue may cause the ruler measurement to be inaccurate.
Official ID Z-3030-2026 · Official record ↗
FUJIFILM Healthcare Americas recalls
Recall found. FUJIFILM Healthcare Americas is named in FDA Class II recall Z-3030-2026 covering FUJIFILM Synapse PACS software v7. Hazard: Software issue may cause the ruler measurement to be inaccurate. Identifying details: UDI (01)00854904006008(10)0704310, Serial Numbers: CV-00272120, CV-0080080176, CV-01318490, CV-01-80102732, CV-80057523, CV-00494020-38. Status: Ongoing.
Models with recalls
All FUJIFILM Healthcare Americas recalls
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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.