Surgical Theater recalls software version SRP.7.12.0 for misalignment risks during 2D Image Fusion. Affected units may need correction to prevent imaging errors.
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 (SRP.7.12.0) for a potential misalignment issue in imaging systems. This could cause secondary images to appear incorrectly layered over primary images during certain procedures.
The software anomaly can cause secondary image layers to misalign with primary layers when large rotational alignment values are applied in 2D Image Fusion. This may lead to incorrect imaging results during medical procedures.
Healthcare professionals using the SuRgical Planner software version SRP.7.12.0 for medical imaging. Those performing procedures requiring precise image alignment are most at risk.
Check for the software version SRP.7.12.0 on the SuRgical Planner system. The unique identifier (UDI/DI) 00863157000336 is associated with this version.
Verify the software version on your SuRgical Planner system to see if it is SRP.7.12.0.
The recall record does not specify current usage status.
Check for the software version SRP.7.12.0 on your SuRgical Planner system.
The recall record does not specify a remedy for this software version.
We’ve drafted a message you can send Surgical Theater to request your refund or repair — edit it as you like.
Subject: Recall Z-0319-2026 — Surgical Theater Surgical Theater Hello, I own a Surgical Theater that is covered by recall Z-0319-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.