On July 17th, the @US_FDA identified a Class I Recall, the most serious type of recall: Teleflex Recalls NEONATAL ConchaSmart Breathing Circuit Due to Circuit Cracks- https://go.usa.gov/xypjr   #FDA #MedicalDevicepic.twitter.com/EUaOIHvIA2

On July 17th, the @US_FDA identified a Class I Recall, the most serious type of recall: Teleflex Recalls NEONATAL ConchaSmart Breathing Circuit Due to Circuit Cracks- https://go.usa.gov/xypjr  #FDA #MedicalDevice pic.twitter.com/EUaOIHvIA2

Source: Food and Drug Adminstration (FDA): CDRHNew - July 18, 2019 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news