FDA Adverse Event Malfunction Summary report: N

DIMENSION VISTA® SYSTEM

MDR report key: 5231890 · Received November 17, 2015

Report

Report Number
9610806-2015-00058
Event Type
Malfunction
Date Received
November 17, 2015
Date of Event
October 16, 2015
Report Date
October 20, 2015
Manufacturer
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
Product Code
JZG
PMA / PMN Number
K083463
Removal / Correction Number
Z-2450-2015
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IT
Reporter Occupation
MEDICAL TECHNOLOGIST

Narratives

Additional Manufacturer Narrative · 1

SIEMENS HEALTHCARE DIAGNOSTICS HAS CONFIRMED COMPLAINTS OF HAS CONFIRMED AN INCREASE IN THE RATE OF "ABNORMAL ASSAY" ERRORS AND CALIBRATION FAILURES WITH THE DIMENSION VISTA B2MIC FLEX REAGENT CARTRIDGE LOTS 15175MA, 15204MA, 15246MA AND 15267MA. THE ERRORS CAN OCCUR ON CALIBRATION, QC AND/OR PATIENT SAMPLES. AS STATED IN THE DIMENSION VISTA OPERATOR'S GUIDE, RESULTS WITH "ABNORMAL ASSAY" FLAGS ARE NOT REPORTABLE. SIEMENS ISSUED AN URGENT MEDICAL DEVICE RECALL COMMUNICATION (B)(4) DATED NOVEMBER 2015 TO CUSTOMERS WHO HAD ORDERED THE IMPACTED LOTS ADVISING THEM TO DISCONTINUE THE USE OF THE LOT.

Description of Event or Problem · 1

THE CUSTOMER COMPLAINED OF OBTAINING ABNORMAL ASSAY E143 FLAGS ON CALIBRATION SAMPLES WITH THE BETA-2 MICROGLOBULIN (B2MIC) FLEX (R) REAGENT CARTRIDGE LOT 15246MA ON THE DIMENSION VISTA INSTRUMENT. THERE IS NO INDICATION THAT PATIENT TREATMENT WAS ALTERED OR PRESCRIBED ON THE BASIS OF THE ABNORMAL ASSAY FLAGS ON B2MIC RESULTS. THERE IS NO INDICATION OF ADVERSE PATIENT IMPACT DUE THE ABNORMAL ASSAY FLAGS ON B2MIC RESULTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
760113 DIMENSION VISTA® SYSTEM B2MIC FLEX® REAGENT CARTRIDGE AND URINE STABILIZER JZG SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH

Patients

Seq Age Sex Outcome Treatment
1