#ICYMI: On February 14th, @US_FDA identified a Class I Recall, the most serious type of recall: Medtronic, Inc. Recalls Dual Chamber Implantable Pulse Generators (IPGs) Due to Possible Circuit Error. Find out more about the recall: https://go.usa.gov/xEUhq   #MedicalDevice #FDApic.twitter.com/YNkrpGSOhH

#ICYMI: On February 14th, @US_FDA identified a Class I Recall, the most serious type of recall: Medtronic, Inc. Recalls Dual Chamber Implantable Pulse Generators (IPGs) Due to Possible Circuit Error. Find out more about the recall: https://go.usa.gov/xEUhq  #MedicalDevice #FDA pic.twitter.com/YNkrpGSOhH

Source: Food and Drug Adminstration (FDA): CDRHNew - February 15, 2019 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news