On June 1st, the @US_FDA identified a Class I Recall, the most serious type of recall: Medtronic recalls StealthStation auto-registration feature due to inaccuracies during deep brain stimulation (DBS) procedures.pic.twitter.com/mGsbP4C8be

On June 1st, the @US_FDA identified a Class I Recall, the most serious type of recall: Medtronic recalls StealthStation auto-registration feature due to inaccuracies during deep brain stimulation (DBS) procedures. pic.twitter.com/mGsbP4C8be

Source: Food and Drug Adminstration (FDA): CDRHNew - June 3, 2020 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news