Model Number 383556 |
Device Problem
Difficult or Delayed Activation (2577)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 02/08/2023 |
Event Type
malfunction
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Event Description
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It was reported while using bd nexiva single port with maxzero, 20g x 1.0" the needle was difficult to disengage.There was no report of patient impact.The following information was provided by the initial reporter: they were unable to disconnect the grey hub from the inserted cannula and had to remove it from the patient and restart with a different catheter.
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Manufacturer Narrative
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Date of event is unknown; awareness date has been used for this field.A device evaluation and/or device history review is anticipated but is not complete.Upon completion, a supplemental report will be filed.
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Event Description
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It was reported while using bd nexiva single port with maxzero, 20g x 1.0" the needle was difficult to disengage.There was no report of patient impact.The following information was provided by the initial reporter: they were unable to disconnect the grey hub from the inserted cannula and had to remove it from the patient and restart with a different catheter.
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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.A review of the device history record was performed and no quality issues were found during production.
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Search Alerts/Recalls
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