Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Becton Dickinson recalls Alaris Infusion Sets for the Alaris Pump Model 8100 due to potential for tube collapse that may cause issues with medication delivery https://go.usa.gov/xypDT   #MedicalDevicepic.twitter.com/9bLlPV6YPe

Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Becton Dickinson recalls Alaris Infusion Sets for the Alaris Pump Model 8100 due to potential for tube collapse that may cause issues with medication delivery https://go.usa.gov/xypDT  #MedicalDevice pic.twitter.com/9bLlPV6YPe

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