Catalog Number CS-22142-CF |
Device Problems
Contamination (1120); Device Damaged Prior to Use (2284)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 12/26/2023 |
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 "the catheter was opened on the table and a foreign object was observed in the lumen, so another catheter must be passed." the malfunction occured prior to patient use.No patient harm or injury.
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Event Description
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It was reported "the catheter was opened on the table and a foreign object was observed in the lumen, so another catheter must be passed." the malfunction occured prior to patient use.No patient harm or injury.
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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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