ABBOTT DIAGNOSTICS SCARBOROUGH, INC. BINAXNOW COVID-19 AG SELF TEST 2CT; CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
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Catalog Number 195-160 |
Device Problem
Non Reproducible Results (4029)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 09/14/2023 |
Event Type
malfunction
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Manufacturer Narrative
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D4 udi: (b)(4).The investigation remains in progress.A supplemental report will be provided after completion or upon receipt of new information.H3 other text : single-use, device discarded.
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Event Description
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The consumer reported conflicting results with two binaxnow covid-19 antigen self tests performed on (b)(6) 2023.The result from the first test was positive.The repeat test generated a negative result.No additional patient information, including treatment and outcome, was provided.
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Manufacturer Narrative
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D4 udi: (b)(4).Testing was performed at abbott diagnostics scarborough, inc.On retained kit lot 209368 with internal positive quality control samples and negative quality control swabs.All test results were valid and performed as expected.Additionally, the manufacturing records and quality control release testing was reviewed for test kit part number 195-160 / lot 209368, test base part number 195-430h / lot 204678.The lot met the required release specifications.A review of the complaints reported as false positive and false negative patient results (confirmed and unconfirmed, conflicting results) related to kit lot 209368 showed that the complaint rate is (b)(4) respectively.In conclusion, abbott diagnostics scarborough was unable to determine the exact root cause of the reported issue.H3 other text : single-use, device discarded.
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Event Description
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The consumer reported conflicting results with two binaxnow covid-19 antigen self tests performed on (b)(6) 2023.The result from the first test was positive.The repeat test generated a negative result.No additional patient information, including treatment and outcome, was provided.
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Search Alerts/Recalls
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