FDA Adverse Event Injury Summary report: N

GS HIV COMBO AG/AB EIA

MDR report key: 7504774 · Received May 10, 2018

Report

Report Number
3022521-2018-00002
Event Type
Injury
Date Received
May 10, 2018
Date of Event
April 10, 2018
Report Date
May 10, 2018
Manufacturer
BIO-RAD LABORATORIES
Product Code
MZF
UDI-DI
00847865010658
PMA / PMN Number
BP100064
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Description of Event or Problem · 1

BIO-RAD TECHNICAL SUPPORT WAS CONTACTED BY (B)(6) HOSPITAL ON 4/12/2018, TO REPORT THAT ON (B)(6) 2018 A PATIENT SAMPLE WAS TESTED WITH GS HIV COMBO AG/AB EIA (LOT 159MJJ-02, EXP. 06/08/2018), WHICH GAVE AN INITIAL (B)(6). THE SAMPLE WAS THEN REPEATED ON (B)(6) 2018 IN DUPLICATE WITH GS HIV COMBO AG/AB EIA (LOT 159MJJ-02, EXP. 06/08/2018); BOTH RESULTS WERE (B)(6). THE INITIAL SAMPLE WAS ALSO TESTED ON (B)(6) 2018 ON THE GEENIUS WHICH SHOWED (B)(6) PRESENT, (B)(6) AS THE FINAL INTERPRETATION. THE CUSTOMER REPORTED THAT THE PATIENT WAS ADMITTED TO THE PSYCHIATRIC UNIT DUE TO HER REACTION AFTER RECEIVING THE INITIAL (B)(6) TEST RESULTS. THE CUSTOMER ALSO REPORTED THAT THE PATIENT IS/HAS BEEN A PSYCHIATRIC PATIENT. THE PATIENT REQUESTED A RETEST, AND WAS REDRAWN ON (B)(6) 2018. THE RESULTS FOR THE SECOND SAMPLE FOR GS HIV COMBO AG/AB EIA (LOT 101NJJ-02, EXP. 01/12/2018) GAVE (B)(6) RESULTS. THE CUSTOMER HAD A THIRD SAMPLE COLLECTED FROM THE PATIENT ON (B)(6) 2018, WITH A PSEUDO CHAIN OF CUSTODY. THE RESULTS FOR THE THIRD SAMPLE FOR GS HIV COMBO AG/AB EIA (LOT 101NJJ-02, EXP. 01/12/2018) GAVE (B)(6) RESULTS. NAT TESTING WAS PERFORMED ON THE SECOND AND THIRD SAMPLES COLLECTED FROM THE PATIENT, WHICH GAVE THE RESULTS OF NOT DETECTED. THE CUSTOMER REPORTED THAT THE PATIENT HAS BEEN INFORMED THAT THEY ARE (B)(6). THE CUSTOMER PERFORMED AN INVESTIGATION TO DETERMINE IF THE SAMPLE WAS MISLABELED, AND WAS UNABLE TO FIND SUBSTANTIAL EVIDENCE THAT THE SAMPLE WAS MISLABELED. AN INVESTIGATION USING SERIAL DILUTION ON GS HIV COMBO AG/AB EIA, GEENIUS HIV-1/2 ASSAY, AND HIV-1 WESTERN BLOT, BY BIO-RAD LABORATORIES PRODUCT SUPPORT, ON THE SAMPLES PROVIDED BY THE CUSTOMER WAS ABLE TO DETERMINE THAT THE INITIAL SAMPLE WAS MORE THAN LIKELY COMPROMISED SOMETIME DURING THE SAMPLE HANDLING PROCESS, AND IS A (B)(6) RESULT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
347694 GS HIV COMBO AG/AB EIA HIV COMBO MZF BIO-RAD LABORATORIES 159MJJ-02 00847865010658

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization