FDA Adverse Event Malfunction Summary report: N

IMMULITE 2000 PROSTATE SPECIFIC ANTIGEN

MDR report key: 3212084 · Received July 8, 2013

Report

Report Number
2432235-2013-00228
Event Type
Malfunction
Date Received
July 8, 2013
Date of Event
May 22, 2012
Report Date
June 13, 2013
Manufacturer
SIEMENS HEALTHCARE DIAGNOSTICS INC.
Product Code
MTF
PMA / PMN Number
P930027
Removal / Correction Number
2432235-06/25/13-003-R
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WV, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

SIEMENS HAS INVESTIGATED THE INCIDENCE OF POSITIVE BIAS ON IMMULITE 2000 PSA ASSAY, AND A POSITIVE BIAS OF 20-23 PERCENT RELATIVE TO WHO 96/670 HAS BEEN CONFIRMED. AN URGENT MEDICAL DEVICE RECALL (UMDR) - UMDR 2013-06-25 IMMULITE/ IMMULITE 1000/ IMMULITE 2000/ IMMULITE 2000 XPI PSA POSITIVE BIAS TO WHO 96/670 - WAS SENT TO CUSTOMERS IN JUNE 2013. THE UMDR STATES THAT CUSTOMERS ARE TO DISCONTINUE USE OF THE PRODUCT AND DISCARD AFFECTED KITS REMAINING IN THEIR INVENTORY. THE CAUSE OF THE POSITIVE BIAS ON THE IMMULITE 2000 PSA ASSAY IS A CONTROL SYSTEM DEFICIENCY.

Description of Event or Problem · 1

THE CUSTOMER HAS OBSERVED HIGH BIAS ON QUALITY CONTROLS FOR THE IMMULITE PROSTATE SPECIFIC ANTIGEN ASSAY WHEN USING REAGENT LOT 104. THE ASSAY WAS RUN ON AN IMMULITE 2000 INSTRUMENT. ALL THREE LEVELS OF QUALITY CONTROLS WERE OUT OF RANGE DURING AN INITIAL RUN. THE CUSTOMER READJUSTED THE ASSAY AND THEN RERAN THE QUALITY CONTROLS, AND LEVELS 2 AND 3 REMAINED OUT OF RANGE HIGH. THERE ARE NO REPORTS OF PATIENT INTERVENTION OR ADVERSE HEALTH CONSEQUENCES DUE TO THE HIGH BIAS ON THE QUALITY CONTROLS FOR THE PSA ASSAY WHEN USING REAGENT LOT 104.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
309064 IMMULITE 2000 PROSTATE SPECIFIC ANTIGEN IMMULITE 2000 PROSTATE SPECIFIC ANTIGEN MTF SIEMENS HEALTHCARE DIAGNOSTICS INC. IMMULITE 2000 PROSTATE SPECIFIC ANTIGEN 104

Patients

Seq Age Sex Outcome Treatment
1