Catalog Number 38831114 |
Device Problem
Device Damaged Prior to Use (2284)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 09/26/2022 |
Event Type
malfunction
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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.Initial reporter first name: (b)(6).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¿ iv catheter experienced a damaged catheter tip.The following information was provided by the initial reporter: a new catheter was opened and observed with damaged plastic tip.
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Manufacturer Narrative
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H6: investigation summary: there was no sample or photo available to bd for evaluation.Therefore, bd was unable to perform a thorough investigation to verify the reported issue.Since, an investigation could not be performed bd was unable to determine a possible root cause.The manufacturing facility has been notified of this incident and the findings.A review of the device history record was performed and no quality issues were found during production.
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Event Description
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It was reported that the bd insyte¿ iv catheter experienced a damaged catheter tip.The following information was provided by the initial reporter: a new catheter was opened and observed with damaged plastic tip.
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Search Alerts/Recalls
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