Surgical Theater recalls SyncAR SNAP software version 1.12.0 for potential misalignment of secondary image layers during 2D Image Fusion. 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 their SyncAR SNAP software version 1.12.0 due to a software anomaly that could cause secondary image layers to misalign with the primary image layer during 2D Image Fusion. This could affect surgical navigation accuracy if large rotational alignment values are applied.
The software anomaly may cause 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 navigation if the misalignment occurs during use.
Surgical staff using SyncAR SNAP software version 1.12.0 for imaging processing. The risk is low as the issue only occurs under specific conditions and does not cause immediate injury.
Check for SyncAR SNAP software version SNP.1.12.0 on the device. The product was sold with UDI/DI 00860003884102.
Verify the software version on your SyncAR SNAP device to see if it is SNP.1.12.0.
The software anomaly may cause image misalignment under specific conditions, but it does not cause immediate injury or death.
Check for software version SNP.1.12.0 on your SyncAR SNAP device. The product was sold with UDI/DI 00860003884102.
The recall does not specify a remedy, so you should check for updates or contact Surgical Theater for guidance.
We’ve drafted a message you can send Surgical Theater to request your refund or repair — edit it as you like.
Subject: Recall Z-0322-2026 — Surgical Theater Surgical Theater Hello, I own a Surgical Theater that is covered by recall Z-0322-2026 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.
