Catalog Number 256094 |
Device Problem
Device Markings/Labelling Problem (2911)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 08/28/2023 |
Event Type
malfunction
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Event Description
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It was reported that while using bd veritor ¿ at-home covid-19 test, there was incorrect expiration date beyond specified shelf life of one kit.No patient impact reported.The following information was provided by the initial reporter: "customer attempted to use product.App alerted customer that the test was expired.Informed customer that expiration can be found on the box.".
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Manufacturer Narrative
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D.4.Medical device lot #: unknown.D.4.Medical device expiration date: unknown.E.1.Initial reporter state: md has been chosen as customer address is unknown.H.3.A device evaluation and/or device history review is anticipated but is not complete.Upon completion, a supplemental report will be filed.H.4.Device manufacture date: unknown.
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Manufacturer Narrative
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After further evaluation of the complaint, it has been determined that the previously submitted report 1119779-2023-00963 was sent in error.There was no report of serious injury, medical intervention, or reportable device malfunction.Therefore, this is not considered to be a reportable malfunction.
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Event Description
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It was reported that while using bd veritor ¿ at-home covid-19 test, there was incorrect expiration date beyond specified shelf life of one kit.No patient impact reported.The following information was provided by the initial reporter: "customer attempted to use product.App alerted customer that the test was expired.Informed customer that expiration can be found on the box.".
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Search Alerts/Recalls
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