This is an initial final report. this issue does not meet reportability criteria; however, it is being reported to fda as the complaint was received via user report.If the product is returned, a physical investigation will be performed and a follow-up report submitted.Three sensors (serial numbers unknown) were reported and have been captured under this submission.The device manufacturing date is unknown.The date entered in is the date abbott diabetes care became aware of the event.All pertinent information available to abbott diabetes care has been submitted.
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