Surgical Theater recalls software version SNP.3.12.0 of their PE SNAP imaging system due to potential misalignment of secondary image layers under specific rotational conditions. Affected units may require correction to prevent imaging errors during surgery.
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 is recalling a specific software version of their PE SNAP imaging system because it can misalign secondary images with the primary image when certain rotational settings are used. This could lead to inaccurate surgical imaging if not corrected.
The software anomaly causes secondary image layers to misalign with the primary image when large rotational alignment values are applied in 2D Image Fusion. This could result in inaccurate surgical imaging if the system is used without correction.
Surgical teams using the PE SNAP software version SNP.3.12.0 for imaging during procedures are most at risk if they encounter specific rotational alignment settings.
Check for the software version SNP.3.12.0 on the PE SNAP imaging system. The unique identifier (UDI/DI) 00863157000374 is associated with this specific version.
Verify the software version on your PE SNAP system to see if it is SNP.3.12.0.
The software version SNP.3.12.0 may cause misalignment of secondary image layers under specific rotational conditions, but it is not immediately hazardous to users.
Check your software version; if it is SNP.3.12.0, contact Surgical Theater for guidance on potential corrections.
Look for the software version SNP.3.12.0 on your PE SNAP system, or check the unique identifier (UDI/DI) 00863157000374.
We’ve drafted a message you can send Surgical Theater to request your refund or repair — edit it as you like.
Subject: Recall Z-0321-2026 — Surgical Theater Surgical Theater Hello, I own a Surgical Theater that is covered by recall Z-0321-2026 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.
