Model Number 405828 |
Device Problem
Disconnection (1171)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/12/2023 |
Event Type
malfunction
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Manufacturer Narrative
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Medical device expiration date: unknown.A device evaluation is anticipated but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.Device manufacture date: unknown.
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Event Description
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It was reported that the bd® combined spinal epidural tray catheter and nexus catheter disconnected during use.This occurred with 3 catheters.The following information was provided by the initial reporter: "nexus catheter disconnected from the epidural catheter despite the clinician securing during placement.This is the third incident in the past week.".
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Manufacturer Narrative
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H6: investigation summary no photos or physical samples that display the reported condition were available for investigation.A device history review could not be completed as no batch number was provided.Based on the available information we are not able to identify a root cause at this time.H3 other text : see h10.
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Event Description
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It was reported that the bd® combined spinal epidural tray catheter and nexus catheter disconnected during use.This occurred with 3 catheters.The following information was provided by the initial reporter: "nexus catheter disconnected from the epidural catheter despite the clinician securing during placement.This is the third incident in the past week.".
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Search Alerts/Recalls
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