Surgical Theater Inc recalls SNAP software version 3.12.0 due to potential misalignment of secondary image layers during 2D Image Fusion. Affected units have UDI/DI 00863157000305.
A software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any secondary image layer(s) to the primary image layer.
Surgical Theater Inc is recalling their SNAP software version 3.12.0 because it may misalign secondary image layers when specific rotational alignment values are applied. This could affect surgical procedures by causing inaccurate imaging during operations.
The software anomaly causes secondary image layers to misalign with the primary image layer when large rotational alignment values are applied in 2D Image Fusion. This could lead to inaccurate surgical imaging but only under specific technical conditions.
Surgical professionals using the SNAP system with software version SNP.3.12.0 are likely affected. The risk is low as the issue only occurs under specific technical conditions during image fusion.
Check for the software version SNP.3.12.0 on the SNAP system. Affected units have the UDI/DI code 00863157000305.
Verify your SNAP system software version is SNP.3.12.0.
The recall states the software may cause misalignment under specific conditions, but it is not explicitly stated whether it is safe to use.
The recall does not specify a remedy, so no action is required beyond checking your software version.
Check for the software version SNP.3.12.0 and the UDI/DI code 00863157000305 on your SNAP system.
We’ve drafted a message you can send Surgical Theater to request your refund or repair — edit it as you like.
Subject: Recall Z-0320-2026 — Surgical Theater Surgical Theater Hello, I own a Surgical Theater that is covered by recall Z-0320-2026 from Surgical Theater. 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.
