PRISM HIV O PLUS
Report
- Report Number
- 1415939-2011-00055
- Event Type
- Malfunction
- Date Received
- February 24, 2011
- Date of Event
- January 24, 2011
- Report Date
- January 28, 2011
- Manufacturer
- ABBOTT LABORATORIES
- Product Code
- MZF
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FR
- Reporter Occupation
- OTHER
Narratives
(B)(4). EVALUATION: US PRODUCT NOT AFFECTED BY THIS ISSUE. FA28MAR2011 WAS ISSUED FOR FALSELY ELEVATED (B)(6) RATES AND DECREASED SPECIFICITY FOR PRISM HIV O PLUS, LIST 3D34-48, LOTS 94737HN00 AND 96484HN00. THE INVESTIGATION HAS DETERMINED THAT THE US-DISTRIBUTED PRODUCT, LIST 3L68-68, IS NOT AFFECTED BY THIS ISSUE AND IS NOT WITHIN THE SCOPE OF THIS ACTION. THE CAUSATIVE AGENT WAS DETERMINED TO BE A SPECIFIC LOT OF ANTIGEN USED TO MANUFACTURE THE P41 PROBE USED IN THESE TWO LOTS OF PRISM HIV O PLUS, LIST 3D34-48 REAGENT. THIS MANUFACTURING ISSUE AFFECTED NON-US PRODUCT ONLY, AS THIS ANTIGEN IS NOT USED IN THE US-DISTRIBUTED PRODUCT.
(B)(4). AN INVESTIGATION IS IN PROCESS. A FOLLOWUP REPORT WILL BE SUBMITTED WHEN THE INVESTIGATION IS COMPLETE. THIS REPORT IS BEING FILED ON AN INTERNATIONAL PRODUCT, LIST NUMBER (B)(4) THAT HAS A SIMILAR PRODUCT DISTRIBUTED IN THE US, LIST NUMBER (B)(4).
THE ACCOUNT STATED THAT FALSE (B)(6) PRISM HIV O PLUS RESULTS WERE GENERATED. THE PATIENT WAS (B)(6) WHEN TESTED WITH SIEMENS ENZYGNOST HIV INTEGRAL II. PRISM HIV GROUP O PLUS: INITIAL RESULT: (B)(6), RETEST 1: (B)(6), RETEST 2: (B)(6). SIEMENS ENZYGNOST HIV INTEGRAL II: (B)(6). THERE WAS NO REPORT OF IMPACT TO PATIENT MANAGEMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PRISM HIV O PLUS | FOR THE DETECTION OF HIV-1 AND HIV-2 ANTIBODIES | MZF | ABBOTT LABORATORIES | 94737HN00 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | ABBOTT PRISM ANALYZER 6A36-04 SN (B)(4)| ABBOTT PRISM ANALYZER 6A36-04 SN (B)(4) |