Surgical Theater recalls EndoSNAP software version SNP.1.12.0 due to potential misalignment of image layers under specific rotational conditions. Affected units may require software update or correction.
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 EndoSNAP imaging system because it can misalign secondary image layers 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 layer when large rotational alignment values are applied in 2D Image Fusion. This could result in inaccurate surgical imaging if the misalignment occurs during use.
Surgical professionals using EndoSNAP software version SNP.1.12.0 for imaging. Those with the specific UDI/DI number 00863157000329 are most at risk.
Check for the software version SNP.1.12.0 on the EndoSNAP system. The unique identifier (UDI/DI) 00863157000329 identifies affected units.
Verify the software version on your EndoSNAP system to see if it is SNP.1.12.0.
Reach out to Surgical Theater Inc for guidance on correcting the software anomaly.
The software anomaly can cause image misalignment under specific rotational conditions, but it does not cause immediate harm. The risk is low and requires specific use conditions.
Check for the software version SNP.1.12.0 and the unique identifier 00863157000329 on your system.
Contact Surgical Theater Inc directly for instructions on correcting the software anomaly.
We’ve drafted a message you can send Surgical Theater to request your refund or repair — edit it as you like.
Subject: Recall Z-0323-2026 — Surgical Theater Surgical Theater Hello, I own a Surgical Theater that is covered by recall Z-0323-2026 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.
