DUBLIN - September 12, 2017 - Medtronic plc (MDT) today announced the global launch of the StealthStation(TM) ENT, a new surgical navigation system designed for surgeons treating conditions within the ...

FDA has classified the recent recall of Medtronic's MDT StealthStation auto-registration feature for deep brain stimulation (DBS) procedures as Class I due to health risks associated with its use.

If Medtronic is currently experiencing a sense of déjà vu, it’s for good reason. About three years after launching a Class I recall of some of its StealthStation surgical navigation software, the ...

Medtronic Plc (NYSE:MDT) has initiated a recall for some versions of its StealthStation S8 application. The FDA deemed software recall as Class I, the most serious kind. The medical device giant is ...

DUBLIN and LOS ANGELES - April 24, 2017 - Medtronic plc (MDT) today launched its new StealthStation(TM) technology at the American Academy of Neurological Surgeons (AANS) annual conference in Los ...

Once again, Medtronic has issued a product correction for its surgical navigation software, earning the StealthStation platform its fifth Class I recall categorization from the FDA in as many years.

As a major development in its Ear, Nose & Throat (ENT) products business, Medtronic plcMDT recently launched StealthStation ENT. This FDA approved and CE Marked surgical navigation system allows ...

BioWorld - Tuesday, August 4, 2026 View BioWorld MedTech Home » Software issues in Medtronic’s Stealthstation system prompts recall To read the full story, subscribe or sign in.

Medtronic plc today launched its new StealthStation™ technology at the American Academy of Neurological Surgeons (AANS) annual conference in Los Angeles. StealthStation technology has been a mainstay ...

Medtronic has recalled the auto-registration feature in the StealthStation deep brain stimulation (DBS) software because of inaccuracies during DBS procedures, according to a notice on the US Food and ...

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