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

Recall Z-2707-2020 — StealthStation" S7 System with Polaris Spectra Camera part number PSU 9733437 - Product Usage: are intended as an aid for precisely locating anatomical structures in either open or percutaneous procedures.

U.S. FDA — Device Enforcement · United States · 2020-06-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2707-2020
Date of alert
2020-06-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Navigation, Inc.
Product category
device
Product type
Devices
Reported risk: There is a potential for specific camera units to be affected by a characterization issue during manufacturing that results in inaccurate navigation while utilizing both the active and passive trackers simultaneously. While no injuries or illnesses have been reported, If impacted cameras were to be used with both active and passive trackers simultaneously, it would result in system navigation inaccuracy of 6mm.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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