Home / Recalls / Medical Devices
Surgical Theater Inc recalls Surgical Planner, BrainSTORM, software version BST.9.3.0, orthopedic augmented reality
Recalled November 5, 2025 · FDA recall Z-0325-2026 · Surgical Theater
Hazard
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. · FDA Class II
Units
3 units
Sold at
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.
Description
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.
Product
Surgical Planner, BrainSTORM, software version BST.9.3.0, orthopedic augmented reality
Manufacturer(s)
Surgical Theater Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →