FUJIFILM Healthcare Americas Corporation recalls FUJIFILM Synapse PACS software v7.4.310
- Recalling company
- FUJIFILM Healthcare Americas Corporation
- Product
- FUJIFILM Synapse PACS software v7.4.310; radiological image processing system
- Reason
- Software issue may cause the ruler measurement to be inaccurate.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jul 22, 2026
- Reported
- Sep 2, 2026
- Distribution
- Worldwide - US Nationwide distribution in the states of NY, VA, KS, OR, OH, and the country of Australia.
- Status
- Ongoing
- Quantity
- 6 units
- Lot / codes
- UDI (01)00854904006008(10)0704310, Serial Numbers: CV-00272120, CV-0080080176, CV-01318490, CV-01-80102732, CV-80057523, CV-00494020-38
- Company location
- Lexington, MA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3030-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3030-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.