Avanos medical inc.Received a single report that referenced two different incidences, which were associated with separate units, involving the same patient.This is the first of two reports.Refer to 9611594-2020-00157 for the second report.It was reported that the "balloon was inflated with air, not using distilled water.After that nutrition was injected while the distal end of the tube was in the abdominal cavity.Nutrition came into the abdominal cavity." the user has admitted that their procedure was incorrect.Additional information received 04-aug-2020 indicated the patient had a fever and abdominal pain the day following the event.The patient's current health status is "recovered." additional information received 05-aug-2020 indicated the device is from the "0620" product family, but the exact model number is unknown.
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