Brief: US FDA Classifies Insulet Omnipod Pods Recall As Class I Due To Serious Injury Risk
02/07/2026 18:24
BRIEF-US FDA Classifies Insulet Omnipod Pods Recall As Class I Due To Serious Injury Risk July 2 (Reuters) - 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
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