Model Number 20402 |
Device Problems
No Apparent Adverse Event (3189); Erratic Results (4059)
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Patient Problems
Insufficient Information (4580); No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 12/08/2021 |
Event Type
malfunction
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Event Description
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Reported discrepant sars results for 1 consumer.It is unknown if the consumer was symptomatic.The consumer communicated that they tested negative an unspecified number of times with quickvue otc while testing positive with other brands of otc rapid antigen testing.This product online review was left by the consumer in 2021 but posted to the retail site at a later date.The actual date of occurrence is unknown.The report was obtained from an online review, no further information could be obtained as no customer contact was possible.
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Manufacturer Narrative
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Investigation conclusion: a review of complaint history did not identify any adverse trends.Root cause: insufficient information source: online customer review.
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Manufacturer Narrative
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Correction: g3 - please correct the awareness date to 3/3/2023.
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Search Alerts/Recalls
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