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Catalog Number 5-16035 |
Device Problem
Leak/Splash (1354)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 07/19/2023 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).
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Event Description
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It was reported that "after intubation, y connector was found leaking, physician changed a new one".No patient harm, desaturation, or injury.The patient status is reported as "fine".
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Event Description
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It was reported that "after intubation, y connector was found leaking, physician changed a new one".No patient harm, desaturation, or injury.The patient status is reported as "fine".
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Manufacturer Narrative
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(b)(4).Complaint verification testing could not be performed as it was reported that the sample is not available for return.A device history record review was performed and no relevant findings were identified.Without the device to evaluate the complaint could not be confirmed and the probable cause could not be determined from the available information.Teleflex will continue to monitor and trend for reports of this nature.
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Search Alerts/Recalls
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