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 recalls specific software versions of the Surpria 64 medical imaging device. If the software error occurs during scanning, patients may need additional scans, increasing radiation exposure risk.
The software error (Error 00003050 or 00003052) prevents proper image reconstruction during scans. This causes the device to fail to display raw data in the work list, requiring additional scans to capture images correctly. Each additional scan increases radiation exposure for the patient.
Healthcare providers using the Surpria 64 device with affected software versions. Patients undergoing scans with these devices may face increased radiation exposure if errors occur.
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.
Verify the software version on your Surpria 64 device to see if it is V3.11 or V3.22.
Reach out to FUJIFILM Healthcare Americas Corporation for guidance on next steps if you have the affected software version.
Software versions V3.11 and V3.22 of the Surpria 64 device.
The error may cause the device to fail to reconstruct images properly, requiring additional scans and increasing radiation exposure for patients.
Check for software versions V3.11 or V3.22 and look for the specific serial numbers listed in the recall notice.
We’ve drafted a message you can send FUJIFILM Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1750-2022 — FUJIFILM Healthcare FUJIFILM Healthcare Hello, I own a FUJIFILM Healthcare that is covered by recall Z-1750-2022 from FUJIFILM Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
