Catalog Number 256082 |
Device Problem
Incorrect, Inadequate or Imprecise Result or Readings (1535)
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Patient Problems
No Consequences Or Impact To Patient (2199); No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/02/2021 |
Event Type
malfunction
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Manufacturer Narrative
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Eua # (b)(4).Medical device lot #: 0304302 was reported, however, this is not a lot# manufactured for this product.Medical device expiration date: unknown.(b)(6).A device evaluation is anticipated, but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.Device manufacture date: unknown.(b)(4).
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Event Description
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It was reported while testing for sars-cov-2 2 false positive results were obtained.Confirmatory testing was performed using pcr test method and the result was negative.There was no report of patient impact.Eua # (b)(4).
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Manufacturer Narrative
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H6: investigation summary: this statement is to summarize the investigation results regarding your complaint that alleges false positive results when using kit rapid detection of sars-cov-2 veritor (material # 256082 ), batch number 0304302.Bd quality performs a systematic approach to investigate false positive complaints.This approach involves review of manufacturing batch history records, testing of retention samples, and testing of customer returned samples, if applicable.An investigation was performed on the batch number provided.The reported issue was unable to be confirmed.However, there is a trend against false positive results.Bd has initiated capa (corrective and preventive action) # 1878253 to further investigate.The root cause could not be identified.Bd quality will continue to closely monitor for trends.
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Event Description
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It was reported while testing for sars-cov-2 2 false positive results were obtained.Confirmatory testing was performed using pcr test method and the result was negative.There was no report of patient impact.Eua # (b)(4).
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Search Alerts/Recalls
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