Catalog Number AB-22050-SS |
Device Problems
Fluid/Blood Leak (1250); Tear, Rip or Hole in Device Packaging (2385)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 08/14/2019 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).The device has not been returned for investigation.Teleflex will continue to monitor and trend related events.
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Event Description
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It was reported that while using a nerve block needle this morning while performing an interscalene nerve block on a patient it was noticed that there was fluid leaking from the tubing.The needle was immediately removed.A hole was visualized in the tubing at the hub of the needle.The needle and packaging were saved.Another nurse then reported that last week they had to replace a block needle because air was aspirated.They believed there was a hole in that tubing as well.That needle was not saved unfortunately.
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Manufacturer Narrative
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Qn#(b)(4).After an additional medical review, a determination was made to re-classify the complaint as a malfunction.Complaint(b)(4) is being reported as a malfunction.There was no serious injury.
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Search Alerts/Recalls
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