Model Number 381533 |
Device Problem
Device Contamination with Chemical or Other Material (2944)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 11/18/2021 |
Event Type
malfunction
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Event Description
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It was reported that the bd insyte¿ autoguard¿ shielded iv catheter experienced foreign matter in the fluid path.The following information was provided by the initial reporter: when i went to place an iv today, i pulled the cap off and looked down to check the needle/catheter and there was this orange thing on it.I did not use it on the patient.
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Manufacturer Narrative
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Date of event: unknown.The date received by manufacturer has been used for this field.A device evaluation is anticipated, but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.
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Event Description
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It was reported that the bd insyte¿ autoguard¿ shielded iv catheter experienced foreign matter in the fluid path.The following information was provided by the initial reporter: when i went to place an iv today, i pulled the cap off and looked down to check the needle/catheter and there was this orange thing on it.I did not use it on the patient.
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Manufacturer Narrative
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Date of event: unknown.The date received by manufacturer has been used for this field.A device evaluation is anticipated, but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.
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Event Description
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It was reported that the bd insyte¿ autoguard¿ shielded iv catheter experienced foreign matter in the fluid path.The following information was provided by the initial reporter: when i went to place an iv today, i pulled the cap off and looked down to check the needle/catheter and there was this orange thing on it.I did not use it on the patient.
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Manufacturer Narrative
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Investigation summary since no samples displaying the condition reported were available for examination, we were unable to fully investigate this incident.A device history record review showed no non-conformances associated with this issue during the production of this batch.
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Search Alerts/Recalls
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