As the lot number for the device was provided, a manufacturing review will be performed.The sample was not returned to the manufacturer for inspection/evaluation.Therefore, the investigation of the reported event is inconclusive.Based upon the available information, the definitive root cause for this event is unknown.The instructions for use (ifu) is adequate for the reported device/patient code(s) and provides general instructions for use, as well as warnings, precautions and potential complications associated with the device.Upon receipt of new or additional information, a follow-up report will be submitted as applicable.(expiration date: 09/2020).
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It was reported that approximately six weeks post port implant, the port insertion site allegedly turned green and wound opened up with pus around the site.Therefore, patient was hospitalized and healthcare provider allegedly identified infection.Reportedly, treatment for the infection was provided and the device was removed.The patient was reported as stable.
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