Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Zimmer Biomet Recalls ROSA Brain 3.0 Robotic Surgery System Due to Software Issue that Incorrectly Positions the Robotic Arm. Find out more about the recall: https://go.usa.gov/xpjBr #MedicalDevicepic.twitter.com/ZAVfINitvY
Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Zimmer Biomet Recalls ROSA Brain 3.0 Robotic Surgery System Due to Software Issue that Incorrectly Positions the Robotic Arm. Find out more about the recall: https://go.usa.gov/xpjBr #MedicalDevice pic.twitter.com/ZAVfINitvY
Source: Food and Drug Adminstration (FDA): CDRHNew - Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news