On (b)(6) 2015, it was reported that the patient experienced "bubbling" at the patch insertion site.The patient noted that he went to the physician's office on the morning of (b)(6) 2015, and was told that there was an infection at the insertion site.He said that he was being treated with oral antibiotics.It is unknown if there was user error or malfunction.The patient declined to answer questions for customer support.This complaint is being reported for the following reason: the device may have caused or contributed to an alleged infection at the infusion site.
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