Medical device recalls Moderate risk

Surgical Theater Inc recalls Surgical Navigation Advanced Platform Patient Engagement (PE SNAP), software version SNP.3.12.0, imaging processing rad…

Recall date
September 16, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0321-2026
FDA classification
Class II
Brand / firm
Surgical Theater Inc
Sold / distributed
Worldwide - US Nationwide distribution in the states of MI, FL, DC, MN, CA, TX, NJ, PA, AZ, NY, KY, IN, WV and the countries of Italy, Germany, Israel, UK.

Why it was 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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Surgical Navigation Advanced Platform Patient Engagement (PE SNAP), software version SNP.3.12.0, imaging processing radiological system

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