| Catalog Number |
362760 |
| Medical Device Problem Code |
Incorrect, Inadequate or Imprecise Result or Readings (1535)
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| Health Effect - Clinical Code |
No Clinical Signs, Symptoms or Conditions (4582)
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| Date of Event |
02/25/2025
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Type of Reportable Event
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Malfunction
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Additional Manufacturer Narrative
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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 or Problem Description
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It was reported while using bd vacutainer® cpt¿ cell preparation tube with sodium citrate, an unspecified number of samples had an insufficient cellular pellet after the 2nd wash.There was no health impact or consequences reported.
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Event or Problem Description
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It was reported while using bd vacutainer® cpt¿ cell preparation tube with sodium citrate, an unspecified number of samples had an insufficient cellular pellet after the 2nd wash.There was no health impact or consequences reported.
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Additional Manufacturer Narrative
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Investigation summary: bd had not received any samples for investigation.A total of 55 retained samples were visually inspected, with no issues being identified.Complaints for sample quality are under statistical control for the month of february 2025.At this time, further testing is not indicated.Based on a review of the device history record for the incident lot, all product specifications and requirements for lot release were met.This complaint has not been confirmed for the indicated failure mode: poor barrier separation.No definitive root cause could be determined; however, the complaint entry indicates processing steps may have not been followed.Complaints received for this device and reported condition will continue to be tracked and trended.Information will be captured on trend reports and monitored.Our business team regularly reviews the collected data for the identification of emerging trends.Bd quality will continue to monitor sample quality complaints.
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Search Alerts/Recalls
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