FDA recall record

Medtronic Navigation StealthStation" S7 System with Polaris Spectra Camera part number PSU recall — FDA Z-2707-2020

There is a potential for specific camera units to be affected by a characterization issue during manufacturing that results in inaccurate navigation while…

Class IIclassification
Z-2707-2020official record ID
Aug 5, 2020report date

Recall record at a glance

Official recordZ-2707-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMedtronic Navigation, Inc.
Report dateAug 5, 2020
Recall initiation dateJun 5, 2020
Quantity2
LocationLouisville, CO, United States

Official 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.

Why the product was 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.

Distribution information

US Nationwide distribution including in the states of Alabama and Massachusetts.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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