Catalog Number ES-04301 |
Device Problem
Material Twisted/Bent (2981)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 03/03/2024 |
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: "03 mar 2024, during the insertion, the doctor found the swg kinked during used on the patient." the patient was 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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Event Description
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It was reported that: "(b)(6) 2024, during the insertion, the doctor found the swg kinked during used on the patient." the patient was reported as fine.
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Search Alerts/Recalls
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