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.
[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
Report Number | 1415939-2008-00055 |
MDR Report Key | 1030581 |
Report Source | 04 |
Date Received | 2008-04-16 |
Date of Report | 2008-03-18 |
Date of Event | 2008-02-16 |
Date Mfgr Received | 2008-03-18 |
Date Added to Maude | 2008-07-28 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | SUDARSHAN HEBBAR, MD |
Manufacturer Street | 100 ABBOTT PARK RD. |
Manufacturer City | ABBOTT PARK IL 600646112 |
Manufacturer Country | US |
Manufacturer Postal | 600646112 |
Manufacturer Phone | 8479379677 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HIVAB HIV-1/HIV-2 (RDNA) EIA |
Generic Name | EIA FOR DETECTION OF AB TO HIV I AND II |
Product Code | LRM |
Date Received | 2008-04-16 |
Model Number | NA |
Catalog Number | 3A77-68 |
Lot Number | 59546M100 |
ID Number | NA |
Operator | OTHER |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Implant Flag | N |
Date Removed | B |
Device Sequence No | 1 |
Device Event Key | 1031115 |
Manufacturer | ABBOTT LABORATORIES |
Manufacturer Address | 100 ABBOTT PARK RD. ABBOTT PARK IL 600643500 US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2008-04-16 |