Catalog Number CS-24703-E |
Device Problems
Fluid/Blood Leak (1250); Obstruction of Flow (2423)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 02/01/2024 |
Event Type
malfunction
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Event Description
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It was reported that " the physician performed the procedure, he found a syringe leakage, it suspected that there was an impurity and causing it to be blocked/occluded.No patient harm." the patient's current condition is reproted as "fine".
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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 " the physician performed the procedure, he found a syringe leakage, it suspected that there was an impurity and causing it to be blocked/occluded.No patient harm." the patient's current condition is reported as "fine".
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Manufacturer Narrative
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Qn # (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.If the sample becomes available at a later date a follow up report will be submitted with investigation results.
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Search Alerts/Recalls
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