Today, the @US_FDA identified a Class I Recall, the most serious type of recall: GE Healthcare Recalls CARESCAPE Respiratory Modules Due to Incorrect Oxygen Values.pic.twitter.com/jFl1s95W9w

Today, the @US_FDA identified a Class I Recall, the most serious type of recall: GE Healthcare Recalls CARESCAPE Respiratory Modules Due to Incorrect Oxygen Values. pic.twitter.com/jFl1s95W9w

https://twitter.com/FDADeviceInfo/status/1224794807647850502

Source: Food and Drug Adminstration (FDA): CDRHNew - February 4, 2020 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news

More News: Medical Devices | Respiratory Medicine