Model Number BCS XP SYSTEM |
Device Problem
Low Test Results (2458)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 03/26/2021 |
Event Type
malfunction
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Manufacturer Narrative
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The customer contacted a siemens customer care center (ccc).Quality controls (qc) recovered in range and no instrument errors occurred at the time of the event.No other patient samples were affected.Sample specific issues cannot be ruled out as a potential cause of the event.The reagent used to obtain the von willebrand factor antigen results is a non-siemens reagent and running this reagent on the bcs xp system is a user defined method (udm) that has not been validated by siemens.Siemens is investigating the issue.
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Event Description
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Two discordant, falsely low von willebrand factor activity (vwf ac) results and two discordant, falsely low von willebrand factor antigen (vwf ag) results were obtained on a patient sample on a bcs xp system.The vwf ac results were obtained with bc von-willebrand reagent (lot 557480).The vwf ag results were obtained with a non-siemens reagent.The discordant results were reported to the physician(s).Later the same day, the sample was repeated twice more for vwf ac and twice more for vwf ag.The repeat results recovered higher than the initial low results.The sample was also run for factor viii on the same day.The factor viii results recovered in the normal range and were not considered discordant.The following day, the sample was repeated twice more for vwf ac and twice more for vwf ag on an alternate bcs xp system.The repeat results recovered higher and matched the repeat results from the previous day.A corrected report was issued, but it is unknown which results were included in the corrected report.There are no known reports of patient intervention or adverse health consequences due to the discordant, falsely low von willebrand factor activity and von willebrand factor antigen results.
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Manufacturer Narrative
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Siemens filed the initial mdr 9610806-2021-00041 on 22-apr-2021.Additional information (28-apr-2021): the customer received the affected sample as a frozen aliquot from a different lab, and they are not able to confirm any information from the other lab regarding transport, tube type, centrifuge information or if the sample was double-spun.Siemens confirmed that the customer was using correct reagent handling.Controls being in range, no mechanical errors, acceptable precision and no other samples showing problems indicates that the instrument and reagents were performing acceptably.Inadequate mixing, centrifugation or other mishandling of the sample cannot be ruled out as contributing factors to the discordant results.The issue is sample specific and was limited to one patient sample.The cause of the event is unknown.The system is performing according to specifications.No further evaluation of this device is required.
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Search Alerts/Recalls
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