PlainRecalls
FDA Devices Moderate Class II Terminated

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.

Reported: August 5, 2020 Initiated: June 5, 2020 #Z-2707-2020

Product Description

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.

Reason for Recall

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.

Details

Units Affected
2
Distribution
US Nationwide distribution including in the states of Alabama and Massachusetts.
Location
Louisville, CO

Frequently Asked Questions

What product was recalled?
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.. Recalled by Medtronic Navigation, Inc.. Units affected: 2.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 5, 2020. Severity: Moderate. Recall number: Z-2707-2020.