FDA Adverse Event Malfunction Summary report: N

SYNCHRON CX9 ALX CLINICAL SYSTEM

MDR report key: 1935630 · Received December 22, 2010

Report

Report Number
2050012-2010-01717
Event Type
Malfunction
Date Received
December 22, 2010
Date of Event
December 1, 2010
Report Date
December 1, 2010
Manufacturer
BECKMAN COULTER INC.
Product Code
JJE
PMA / PMN Number
K950958
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SF
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE CUSTOMER WAS SENT REPLACEMENT.

Description of Event or Problem · 1

A CUSTOMER CONTACTED BECKMAN COULTER INC. (BCI) STATING THAT A WASH CONCENTRATE BOTTLE BROKE AND LEAKED IN THE SYNCHRON CX9 ALX CLINICAL SYSTEM. NO INJURY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SYNCHRON CX9 ALX CLINICAL SYSTEM CLINICAL CHEMISTRY ANALYZER JJE BECKMAN COULTER INC. NA NA

Patients

Seq Age Sex Outcome Treatment
1