A customer emailed adc regarding unspecified issues with the adc device.Due to this, the customer experienced a loss of consciousness however, there was no third-party medical intervention provided.No further details were provided.There was no report of death or permanent impairment associated with this event.
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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 it has been determined that there was no indication that the product did not meet specification.A tripped trend review was conducted for the reported complaint and libre sensor and sensor, and 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 date of event is unknown.The date entered is the date abbott diabetes care became aware of the event.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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