HIVAB HIV-1/HIV-2 (RDNA) EIA 3A77-68

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2008-04-16 for HIVAB HIV-1/HIV-2 (RDNA) EIA 3A77-68 manufactured by Abbott Laboratories.

Event Text Entries

[852588] The customer stated a pt generated a false reactive result on hivab hiv-1/hiv-2 (rdna)eia. The pt had four viral immunizations in 2008 and a blood specimen was obtained after the immunizations. The sample was tested the following day and generated repeat reactive results on hiv-1/hiv-2 (rdna eia and was indeterminate on western blot. Add'l samples were obtained from this pt on five days later, and the following month, both generating nonreactive results on hiv-1/hiv-2 (rdna) eia when tested the day after collection. No impact to pt mgmt was reported.
Patient Sequence No: 1, Text Type: D, B5


[8062071] This is an initial report. An investigation is in process. A final report will be submitted when the investigation is completed.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1415939-2008-00055
MDR Report Key1030581
Report Source04
Date Received2008-04-16
Date of Report2008-03-18
Date of Event2008-02-16
Date Mfgr Received2008-03-18
Date Added to Maude2008-07-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactSUDARSHAN HEBBAR, MD
Manufacturer Street100 ABBOTT PARK RD.
Manufacturer CityABBOTT PARK IL 600646112
Manufacturer CountryUS
Manufacturer Postal600646112
Manufacturer Phone8479379677
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHIVAB HIV-1/HIV-2 (RDNA) EIA
Generic NameEIA FOR DETECTION OF AB TO HIV I AND II
Product CodeLRM
Date Received2008-04-16
Model NumberNA
Catalog Number3A77-68
Lot Number59546M100
ID NumberNA
OperatorOTHER
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedB
Device Sequence No1
Device Event Key1031115
ManufacturerABBOTT LABORATORIES
Manufacturer Address100 ABBOTT PARK RD. ABBOTT PARK IL 600643500 US


Patients

Patient NumberTreatmentOutcomeDate
10 2008-04-16

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.