It was reported the patient had his action removed due to infection, diarrhea, exposure, and anal pain.The patient had experienced diarrhea and anal pain; anterior exposure and positive blood cultures were discovered during examination.The action was removed due to infection from exposure.Abdominal adhesions were also discovered.No additional patient complications were reported in relation to this event.
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Additional information: cuff: catalog #: 72401982, expiration date: 4/02/2018, serial #: (b)(4), manufacture date: 4/2013.Pump: catalog #: 72402287, expiration date: 10/09/2014, serial #: (b)(4), manufacture date: 10/2013.Balloon: catalog #: 72402106, expiration date: 04/02/2018, serial #: (b)(4), manufacture date: 04/2013.The explanted action device was visually inspected and functionally tested.The pump performed within specifications.There was a leak in the cuff that was the result of a sharp instrument which probably occurred during removal.The balloon tested at 94.1 cmh2o.It is rated at 101-110 cmh2o.
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