Catalog Number CV-15703 |
Device Problems
Bent (1059); Difficult to Insert (1316)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 02/20/2018 |
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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The customer reports: when catheter is passed, it is observed that the guide is bent, preventing the passage of the catheter.A new attempt is made and it is successful.
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Event Description
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The customer reports: when catheter is passed, it is observed that the guide is bent, preventing the passage of the catheter.A new attempt is made and it is successful.
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Manufacturer Narrative
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(b)(4).Complaint verification testing could not be performed as no sample was returned for analysis.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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