Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SyncAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR SNAP) Recalled by Surgical Theater Inc Due to A software anomaly, under specific conditions when large...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Surgical Theater Inc directly.
Affected Products
SyncAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR SNAP), software version SNP.1.12.0, imaging processing radiological system
Quantity: 14 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Surgical Theater Inc
Surgical Theater Inc has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report