MAUDE Adverse Event Report: ABBOTT DIAGNOSTICS SCARBOROUGH, INC. BINAX NOW COVID-19 AG CARD KIT 40T EUA; CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.

Catalog Number	195-000
Medical Device Problem Code	False Positive Result (1227)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/01/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Correction: b5 - describe event or problem.H11 - b3: the date indicated is an approximation as the exact event date was not provided.Testing was performed at abbott diagnostics scarborough, inc.On retained kit lot 229606y 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 195-000/ lot 229606y and test base part number 195-430h/ lot 225065r.The lot met the required release specifications.A review of the complaints reported false positive patient results (confirmed and unconfirmed, conflicting results) related to kit lot 229606y showed that the complaint rate is (b)(4).Abbott diagnostics scarborough was unable to determine the exact root cause of the reported issue, however it could have possibly been related to the specific patient sample.
Event or Problem Description
The customer reported an unknown number of false positive results with the binax now covid-19 ag card kit performed on unknown dates.The sample and swab types were not provided.This manufacturer's report addresses lot two (2) of two (2).Confirmation pcr (platform - unknown) testing was performed on unknown dates and generated negative results.Although requested, no additional patient information including treatment and outcome, was provided.
Additional Manufacturer Narrative
H11 - b3: the date indicated is an approximation as the exact event date was not provided.The remainder of the investigation remains in progress.A supplemental report will be provided after completion or upon receipt of new information.
Event or Problem Description
The customer reported an unknown number of false positive results with the id now covid-19 2.0 assay performed on unknown dates.The sample and swab types were not provided.This manufacturer's report addresses lot two (2) of two (2).Confirmation pcr (platform - unknown) testing was performed on unknown dates and generated negative results.Although requested, no additional patient information including treatment and outcome, was provided.
Additional Manufacturer Narrative
H11 - b3: the date indicated is an approximation as the exact event date was not provided.Testing was performed at abbott diagnostics scarborough, inc.On retained kit lot 229606y 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 195-000/ lot 229606y and test base part number 195-430h/ lot 225065r.The lot met the required release specifications.A review of the complaints reported false positive patient results (confirmed and unconfirmed, conflicting results) related to kit lot 229606y showed that the complaint rate is (b)(4).Abbott diagnostics scarborough was unable to determine the exact root cause of the reported issue, however it could have possibly been related to the specific patient sample.
Event or Problem Description
The customer reported an unknown number of false positive results with the id now covid-19 2.0 assay performed on unknown dates.The sample and swab types were not provided.This manufacturer's report addresses lot two (2) of two (2).Confirmation pcr (platform - unknown) testing was performed on unknown dates and generated negative results.Although requested, no additional patient information including treatment and outcome, was provided.

• Brand Name: BINAX NOW COVID-19 AG CARD KIT 40T EUA
• Common Device Name: CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
• Manufacturer (Section D): ABBOTT DIAGNOSTICS SCARBOROUGH, INC.; 10 southgate road; scarborough ME 04074
• Manufacturer Contact: rachel blackwell ; 10 southgate road; scarborough, ME 04074 ; 6613888803
• MDR Report Key: 19639221
• Report Number: 1221359-2024-00436
• Device Sequence Number: 7137806
• Product Code: QKP
• UDI-Device Identifier: 10811877011290
• UDI-Public: (01)10811877011290(17)240922(10)229606Y
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: EUA202537
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 07/23/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 09/22/2024
• Device Catalogue Number: 195-000
• Device Lot Number: 229606Y
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/14/2024
• Supplement Date Received by Manufacturer: 07/09/2024; 07/18/2024
• Initial Report FDA Received Date: 06/28/2024
• Supplement Report FDA Received Date: 07/09/2024; 07/23/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 12/19/2023
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown