US FDA:
US FDA - CLASSIFIES INSULET OMNIPOD PODS RECALL AS CLASS I DUE TO SERIOUS INJURY RISK
US FDA - INSULET REPORTS 24 SERIOUS INJURIES, NO DEATHS FROM OMNIPOD PODS ISSUE AS OF MAY 20
Reuters
US FDA Classifies Insulet Omnipod Pods Recall As Class I Due To Serious Injury Risk
US FDA: