FUJIFILM Healthcare recalls SCENARIA View software versions V1.08-V1.09D due to image reconstruction errors that may require additional radiation exposure during 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 Healthcare is recalling specific versions of SCENARIA View software that may cause images to fail reconstruction during scans. This could require patients to undergo additional scans, increasing radiation exposure risk.
The software may generate error codes (00003050 or 00003052) during scans, causing images to not reconstruct properly. This may require additional scans to capture images correctly, potentially increasing radiation exposure for patients.
Patients using SCENARIA View software versions V1.08 through V1.09D with the listed serial numbers are affected. Medical facilities using these software versions are most at risk.
Check if your SCENARIA View software version is V1.08, V1.09B, V1.09C, V1.09D, V1.0B, or V1.0C. The affected units have specific serial numbers listed in the recall notice.
Verify your SCENARIA View software version matches the recalled versions listed in the recall notice.
No, the recall does not require immediate discontinuation. The software may continue to function but could cause image errors requiring additional scans.
If the software generates error codes 00003050 or 00003052, images may not reconstruct properly, potentially requiring additional scans to capture images correctly.
The recall does not specify a remedy, so no action is required beyond checking your software version and serial number.
We’ve drafted a message you can send FUJIFILM Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1748-2022 — FUJIFILM Healthcare FUJIFILM Healthcare Hello, I own a FUJIFILM Healthcare that is covered by recall Z-1748-2022 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.
