Catalog Number CV-17702-E |
Device Problem
Obstruction of Flow (2423)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 08/01/2022 |
Event Type
malfunction
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Event Description
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The complaint is reported as after insertion they found obstruction in both lumen.No patient harm was reported.The patient's condition is reported as fine.
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Manufacturer Narrative
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(b)(4).
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Manufacturer Narrative
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Qn#(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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The complaint is reported as "after insertion they found obstruction in both lumen".No patient harm was reported.The patient's condition is reported as fine.
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Search Alerts/Recalls
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