TERUMO CARDIOVASCULAR SYSTEMS CORPORATION VALVE, O.P.S BULK, N-S; OVERPRESSURE SAFETY VALVE
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Model Number LN130B |
Device Problem
Leak/Splash (1354)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 07/17/2023 |
Event Type
malfunction
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Event Description
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The user facility reported to terumo cardiovascular that during cardiopulmonary bypass, the valve leaked in line 5 from the vent.As per the sales associate, it was quickly clamped and replaced with a single sterile valve and unclamped to continue the procedure.The patient's condition is okay.*no known consequence or health impact to patient, *product was changed out, *there was a blood loss of 50ml, *procedure was completed successfully.
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Manufacturer Narrative
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Terumo has not received the device for evaluation; therefore, the investigation has yet to be completed.Terumo plans on submitting a follow-up report when the investigation is complete and when more information becomes available.For this reason, terumo references evaluation conclusion code 11.Component code: 3094- one-way valve, health effect ¿ impact code: 2199 - no health consequences or impact, health effect ¿ clinical code: 4582 - no clinical signs, symptoms or conditions, medical device problem code: 1354- leak/splash, investigation findings: 3233 - results pending completion of investigation, investigation conclusions: 11 - conclusion not yet available.
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Event Description
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Valve leaked in line 5 from the vent.
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Manufacturer Narrative
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This follow-up report is submitted to fda in accord with applicable regulations.Upon further investigation of the reported event, the following information is new and/or changed: d4 (additional device information - added exp date).G3 (date received by manufacturer).G6 (indication that this is a follow-up report).H2 (follow-up due to additional information and device evaluation).H3 (device evaluated by manufacturer).H4 (device manufacture date).H6 (identification of evaluation codes 10, 3331, 213, 67).Type of investigation #1: 10 - testing of actual/suspected device; type of investigation #2: 3331 - analysis of production records; investigation findings: 213 - no device problem found; investigation conclusions: 67- no problem detected.The returned sample was visually inspected with no anomalies noted on the device.Ops valves are subject to a 100% leak test, which includes five different tests the units are run through to ensure there are no leaks and both the umbrellas and duckbills are functioning properly.The returned sample was leak tested and passed all tests.The evaluation of the unit was found to function as intended and met all of the product specifications.All available information has been placed on file in quality management for appropriate tracking, trending, and follow-up.
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Event Description
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Valve leaked in line 5 from the vent.
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Manufacturer Narrative
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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 august 11, 2023. upon further investigation of the reported event, the following information is new and/or changed: d9 (device availability - added date returned to manufacturer).G3 (date received by manufacturer).G6 (indication that this is a follow-up report).H2 (follow-up due to additional information).H3 (device evaluation anticipated by manufacturer - a second follow-up will be submitted upon completion of the investigation and/or submission of new information, thus tcvs references conclusions code 11.) all available information has been placed on file in quality management for appropriate tracking, trending, and follow-up.
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