Development of infection at the sensor insertion site is a known and anticipated potential adverse effect.User initially reported infection and puss at insertion site to medical provider who advised user to go to the clinic to have the sensor removed.The sensor was removed the same day and a new sensor was inserted into the right arm.User was prescribed antibiotics.A review of the device's manufacturing records revealed that the sensor lot met all requirements including sterilization requirements for release.No further investigation is required.
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