Surgical Theater recalls SpineAR SyncAR SNAP software version SPR.1.2.0 for orthopedic use. A software anomaly may cause misalignment of image layers during surgery, requiring 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 for orthopedic surgery. This software could misalign image layers during procedures if certain rotational settings are used, potentially affecting surgical accuracy.
The software may misalign secondary image layers with the primary image layer when large rotational alignment values are applied in 2D Image Fusion. This could lead to inaccurate surgical guidance during procedures.
Orthopedic surgeons and surgical teams using the SpineAR SyncAR SNAP software version SPR.1.2.0 are affected. Those performing spinal surgeries with this software version are most at risk.
Check for the software version SPR.1.2.0 on the SpineAR SyncAR SNAP platform. The product has a unique identifier (UDI/DI) 00860003884126.
Verify the software version on your SpineAR SyncAR SNAP device to see if it is SPR.1.2.0.
The recall states a software anomaly may cause misalignment of image layers under specific conditions, but does not specify if it causes injury.
The recall does not provide a remedy, so no action is required unless you see the specific software version SPR.1.2.0.
Check for the software version SPR.1.2.0 on your SpineAR SyncAR SNAP device, and look for the unique identifier 00860003884126.
We’ve drafted a message you can send Surgical Theater to request your refund or repair — edit it as you like.
Subject: Recall Z-0324-2026 — Surgical Theater Surgical Theater Hello, I own a Surgical Theater that is covered by recall Z-0324-2026 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.
