Catalog Number 256082 |
Device Problem
Incorrect, Inadequate or Imprecise Result or Readings (1535)
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Patient Problems
No Patient Involvement (2645); No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 10/21/2020 |
Event Type
malfunction
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Manufacturer Narrative
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Eua # (b)(4).Initial reporter state: address information was not able to be obtained.(b)(6) was used as a place holder.A device evaluation is anticipated, but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.(b)(4).
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Event Description
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It was reported while testing for sars-cov-2 a false positive result was obtained.A repeat test was performed using a pcr test method and the result was negative.The customer stated the patient tested was asymptomatic.This test is not intended for use on asymptomatic patients and was therefore used off label.There was no report of patient impact.Eua # (b)(4).
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Manufacturer Narrative
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Eua#: (b)(4).H6: investigation summary bd has received several customer complaints for false positive results, when using bd sars-cov-2 reagents for bd veritor¿ system.The current investigation concerns multiple lots of bd sars-cov-2 reagents for bd veritor¿ system.Bd takes a systematic approach to investigating false positive complaints that are received.This approach involves review of manufacturing batch history records, testing of retention samples, and testing of customer returned samples if applicable.Retain samples were tested for batch #: 0216641.The defect could not be replicated and therefore the complaint could not be confirmed.A device history review was conducted for lot number 0216641.The investigation did not find a root cause for the false positive results that were observed.It is recommended that each customer review their workflow carefully to ensure that the package insert is being followed as written.The root cause is under investigation and will be documented in our quality system.Bd cannot confirm the complaint based on the investigation that was performed.A corrective and preventive action (capa#1878253) is already initiated to investigate the root cause and some mitigation actions are already being addressed.
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Event Description
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It was reported while testing for sars-cov-2 a false positive result was obtained.A repeat test was performed using a pcr test method and the result was negative.The customer stated the patient tested was asymptomatic.This test is not intended for use on asymptomatic patients and was therefore used off label.There was no report of patient impact.Eua # (b)(4).
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Search Alerts/Recalls
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