The product has been requested back for an investigation.At this time product has not yet been returned and a valid serial number has not been provided.An extended investigation has been performed for the reported complaint and there was no indication that the product did not meet specification.A tripped trend review was conducted for the reported complaint and freestyle libre sensors, no trends were identified that would indicate any product related issues.If the product is returned, a physical investigation will be performed and a follow-up report submitted.The device mfg date is unknown.The date entered 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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Customer reported a packaging issue, stating their abbott diabetes care (adc) order contained the incorrect product and were unable to obtain readings or monitor glucose levels.As a result, customer experienced a loss of consciousness and was unable to self-treat, requiring third-party treatment of "sugar drink" orally by emergency services once ambulance arrived.There was no report of death or permanent impairment associated with this event.
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