Catalog Number 393222 |
Device Problem
Material Protrusion/Extrusion (2979)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 02/28/2024 |
Event Type
malfunction
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Manufacturer Narrative
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H.3.If a device evaluation and/or device history review is completed, a supplemental report will be filed.
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Event Description
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It was reported that bd venflon pro safety 22ga 0.9mm od 25mm l needle through catheter.The following information was provided by the initial reporter: when inserting canula to patient, the needle stick through the cannula.When did the incident occur? during use.This has happened to 2 nurses during use and they say it never before has happened to them.
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Manufacturer Narrative
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As no sample and no photo were returned, further investigation cannot be performed.Visual inspection and functional test were performed per control plan during production.Device history record was reviewed, and no abnormality was reported.No similar quality notification was raised for the reported defect in the past 12 months.Therefore, the root cause cannot be determined.Complaint trend would be monitored, and complaint will be reopened when sample is returned.
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Event Description
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When inserting canula to patient, the needle stick through the cannula.When did the incident occur? during use, this has happened to 2 nurses during use and they say it never before has happened to them.
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Search Alerts/Recalls
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