FDA Classifies Insulet Omnipod Pods Recall As Class I Due To Serious Injury Risk; Insulet Reports 24 Serious Injuries, No Deaths From Omnipod Pods Issue As Of May 20

Benzinga Newsdesk www.benzinga.com Neutral 81.2%

Neg 0% Neu 81.2% Pos 0%

https://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/insulin-pump-recall-insulet-removes-omnipod-pods