.@US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall: https://go.usa.gov/xPMEn   #MedicalDevicepic.twitter.com/YU9Iq3Yw0b

. @US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall: https://go.usa.gov/xPMEn  #MedicalDevice pic.twitter.com/YU9Iq3Yw0b

Source: Food and Drug Adminstration (FDA): CDRHNew - November 30, 2018 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news