Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0050-2025 — StealthStation S8 App versions 1.3.0 and 1.3.2, (Model # 9735762) The StealthStation System, with StealthStation Spine software, is intended as an aid for precisely locating anatomical structures in either open or percutaneous neurosurgical and orthopedic procedures.

U.S. FDA — Device Enforcement · United States · 2024-08-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0050-2025
Date of alert
2024-08-22
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Navigation, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00763000456986
Reported risk: Due to two software anomalies that can occur within a spine procedure. Two issues are: 1. Navigation Orientation - when lateral orientation radiographic images are taken, information may appear flipped when utilizing the system (180 degree flipped). 2. Pop-up Message - when using CT+Fluouroscopy images with a slice spacing thickness greater than 2mm, the system does not display a pop-up message indicating the slice spacing is not optimal.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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