Catalog Number 397251 |
Device Problems
Break (1069); Device Operates Differently Than Expected (2913)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 10/18/2017 |
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 during use, a bd connecta¿ extension tube malfunctioned as the connection to the nose piece was damaged.There was no report of injury or medical intervention.
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Manufacturer Narrative
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A sample is not available for evaluation.A review of the device history record revealed no irregularities during the manufacture of the reported lot # 6218889.Conclusion: without a sample, an absolute root cause for this incident cannot be determined.
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Search Alerts/Recalls
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