FDA Adverse Event Malfunction Summary report: N

APPLIED BIOSYSTEMS 7500 FAST DX REAK TIME PCR

MDR report key: 3978887 · Received June 27, 2014

Report

Report Number
3003673482-2014-00020
Event Type
Malfunction
Date Received
June 27, 2014
Date of Event
January 16, 2014
Report Date
January 16, 2014
Manufacturer
LIFE TECHNOLOGIES HOLDINGS PTE LTD
Product Code
NSU
PMA / PMN Number
K082562
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE IS AN INSTRUMENT AND IS NOT IMPLANTED/EXPLANTED. THE REPAIR WAS COMPLETED BY REPLACING THE SAMPLE BLOCK. THE INSTRUMENT PASSED ALL SPECIFICATION TESTS AFTER THE SAMPLE BLOCK WAS REPLACED. THIS DEVICE IS USED TO OBTAIN RESULTS FOR A DIAGNOSIS. DEVICE INTENDED USE: THE APPLIED BIOSYSTEMS 7500 FAST DX REAL-TIME PCR INSTRUMENT WITH THE SDS SOFTWARE VERSION 1.4 IS A REAL-TIME NUCLEIC ACID AMPLIFICATION AND DETECTION SYSTEM THAT MEASURES NUCLEIC ACID SIGNALS FROM REVERSE TRANSCRIBED RNA AND CONVERTS THEM TO COMPARATIVE QUANTITATIVE READOUTS USING FLUORESCENT DETECTION OF DUAL-LABELED HYDROLYSIS PROBES. THE 7500 FAST DX REAL-TIME PCR INSTRUMENT IS TO BE USED ONLY BY TECHNOLOGISTS TRAINED IN LABORATORY TECHNIQUES, PROCEDURES AND ON USE OF THE ANALYZER.

Description of Event or Problem · 1

A CUSTOMER REPORTED A HEATER BLOCK ISSUE ON THE INSTRUMENT APPLIED BIOSYSTEMS 7500 FAST DX (CATALOG NO. 4406985) WITH SERIAL NO. (B)(4), RESULTING IN INCORRECT RESULTS FROM AN ASSAY RUN. NO PT INVOLVEMENT REPORTED. (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
378388 APPLIED BIOSYSTEMS 7500 FAST DX REAK TIME PCR INSRUMENTATION FOR CLINICAL MULTIPL NSU LIFE TECHNOLOGIES HOLDINGS PTE LTD

Patients

Seq Age Sex Outcome Treatment
1