Catalog Number 306547 |
Device Problems
Break (1069); Detachment Of Device Component (1104)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 01/28/2018 |
Event Type
malfunction
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Manufacturer Narrative
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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 posiflush¿ normal saline syringe broke off in arterial line transducer.No injury.Happens when the nurses are monitoring blood pressure.When they have to zero out the line, they hook a saline syringe up to the end to keep it primed.Reported during use.No reports of serious injury or medical intervention.
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Manufacturer Narrative
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Investigation results: since no samples displaying the condition reported are available for examination, we were unable to fully investigate this incident.No root cause can be determined as no samples were received.Complaints received for this device and reported condition will continue to be tracked and trended.Information will be captured on trend reports and monitored monthly.Our business team regularly reviews the collected data for identification of emerging trends.Based on no sample, the investigation concluded, bd was not able to confirm the indicated failure.No device history review was completed as no batch number was provided.
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Search Alerts/Recalls
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