Use cautionMedical device recall · FDA · Published July 12, 2022
FUJIFILM Surpria 64 Software V3.11/V3.22: Radiation Risk During Scans
FUJIFILM recalls Surpria 64 software versions V3.11 and V3.22 due to potential radiation exposure from improper image reconstruction during scans. Affected units may require additional scans.
Error 00003050 or 00003052 may occur during scanning, the captured images will not be reconstructed and the Raw Data will not be displayed in the work list.result, may result in the need for additional scanning to capture the images properly for reconstruction, thereby exposing the patient to additional radiation
“FUJIFILM Surpria 64 Software V3.11/V3.22: Radiation Risk During Scans.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/60372-fujifilm-surpria-64-software-v3-11-v3-22-radiation-risk. Based on FDA recall #Z-1750-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1750-2022%22&limit=1).
The FDA announced on July 12, 2022, that FUJIFILM Healthcare Americas Corporation is recalling Surpria 64 units with software versions V3.11 and V3.22 due to a scanning error that may require additional imaging and expose patients to extra radiation. The agency issued recall number Z-1750-2022 for the voluntary Class II action.
How to tell if you have it
Brand: FUJIFILM Healthcare
Product: Surpria 64, Software Version V3.11, V3.22
UPCs: 04573596200520, 04580292766601
Units affected: 16
The hazard
Error 00003050 or 00003052 may occur during scanning, causing captured images not to be reconstructed and Raw Data not to be displayed in the work list. This error may result in the need for additional scanning to capture the images properly for reconstruction, thereby exposing the patient to additional radiation.
Context
GovInfoNow's records show FUJIFILM Healthcare Americas Corporation has 13 other recalls on record since 2021-10-14. Recent similar recalls include the FUJIFILM Synapse PACS Software v7.4.310 recall (2026-07-22), the FUJIFILM FDR Visionary Suite CH-200 X-ray Device Recall (2026-01-09), and the FUJIFILM FDR Visionary Suite CH-200 X-ray Tube Shaft Break Risk (2025-09-15). Other recent recalls of similar products include the Philips Brilliance CT 64 Medical Scanner Recall (2026-08-07), the Philips IQon Spectral CT Software 4.7.7.x Recall (2026-08-07), and the Philips Spectral CT 7500 Scanner May Cause Extra Radiation Exposure (2026-08-18).
How to tell if you have this one
Check for software versions V3.11 or V3.22 on the Surpria 64 device. Affected units have specific serial numbers listed in the recall notice.
Brand
FUJIFILM Healthcare
Product
Surpria 64: Software Version V3.11, V3.22
Category
Medical device
FDA recall event · 3 products
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1750-2022 (July 12, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1750-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
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