ALERE DETERMINE HIV 1/2 AG/AB COMBO
Report
- Report Number
- 1221359-2018-00050
- Event Type
- Malfunction
- Date Received
- May 11, 2018
- Date of Event
- March 19, 2018
- Report Date
- May 11, 2018
- Manufacturer
- ALERE SCARBOROUGH INC.
- Product Code
- MZF
- UDI-DI
- 10811877010293
- PMA / PMN Number
- BP120037-0
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- OTHER
Narratives
TESTING WAS PERFORMED ON ALERE DETERMINE HIV 1/2 AG/AB COMBO KIT LOT 091045 WITH THE FOLLOWING INTERNAL WHOLE BLOOD CONTROL SAMPLES: (B)(6). ALL TEST RESULTS WERE VALID AND PERFORMED AS EXPECTED. ADDITIONALLY, THE MANUFACTURING BATCH RECORDS FOR LOT 091045 WERE REVIEWED. THIS LOT MET THE REQUIRED RELEASE SPECIFICATIONS. A REVIEW OF THE COMPLAINTS REPORTED (B)(6) OR (B)(6) RELATED TO LOT NUMBER 091045 SHOWED THAT THE COMPLAINT RATE IS (B)(4)%. THE EVIDENCE AVAILABLE DOES NOT INDICATE THAT THE PRODUCT IS PERFORMING OUTSIDE LABEL CLAIMS. ALERE (B)(4) WAS UNABLE TO DETERMINE THE EXACT ROOT CAUSE OF THE REPORTED ISSUE. THE RESULTS OBTAINED MAY POSSIBLY BE RELATED TO THE PATIENT SAMPLE. THE SAMPLE MAY HAVE CONTAINED SPECIFIC SUBSTANCES WHICH MAY HAVE AFFECTED THE RESULTS. THE AVAILABLE EVIDENCE SUGGESTS THAT THIS DEVICE LOT IS PERFORMING WITHIN LABELED CLAIMS.
A (B)(6) RESULT WAS REPORTED ON A SAMPLE TESTED WITH THE ALERE DETERMINE HIV 1/2 AG/AB COMBO. THE TYPE OF CONFIRMATORY TESTING WAS REPORTED AS "CONVENTIONAL" AND THE RESULT WAS REPORTED AS (B)(6) FOR (B)(6). THERE IS INSUFFICIENT INFORMATION TO DETERMINE IF A MALFUNCTION OCCURRED. THE PATIENT GENDER, PREGNANCY STATUS, TREATMENT AND PATIENT OUTCOME WERE UNKNOWN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 350169 | ALERE DETERMINE HIV 1/2 AG/AB COMBO | IVD FOR HIV AG/AB | MZF | ALERE SCARBOROUGH INC. | 091045 | 10811877010293 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |