The user facility reported to terumo cardiovascular that during cardiopulmonary bypass, the oxygenator thermistor was not giving temperature.As per user facility, they monitored the patient's temperature on the cdi 500 blood parameter monitoring device.No known impact or consequence to patient.Product was not changed out.Procedure was completed successfully.
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This follow-up report is submitted to fda in accord with applicable regulations ¿ and as indicated by terumo cardiovascular systems in the initial report submitted to the fda on may 31, 2019. upon further investigation of the reported event, the following information is new and/or changed:.Method code #1: 10 - testing of actual/suspected device.Method code #2: 11 - testing of device from same lot/batch retained by manufacturer.Method code #3: 3331 - analysis of production records.Results code: 3259 - improper physical structure.Conclusions code: 4307 - cause traced to component failure.The affected sample was not returned for evaluation.A retention sample from the same product/lot number combination was tested and found to be functioning properly.An engineering investigation and capa have been initiated to determined a definitive root cause.All available information has been placed on file in quality management for appropriate tracking, trending, and follow-up.
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