FDA Adverse Event Malfunction Summary report: N

SYNCHRON® CX9 PRO CLINICAL SYSTEMS

MDR report key: 1913155 · Received December 2, 2010

Report

Report Number
2050012-2010-01464
Event Type
Malfunction
Date Received
December 2, 2010
Date of Event
October 12, 2010
Report Date
November 9, 2010
Manufacturer
BECKMAN COULTER INC.
Product Code
JJE
PMA / PMN Number
K950958
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SF
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE CUSTOMER WAS SENT A REPLACEMENT.

Description of Event or Problem · 1

A CUSTOMER CONTACTED BECKMAN COULTER INC. (BCI) IN REGARDS TO A BROKEN WASH CONCENTRATE BOTTLE THAT LEAKED WHILE ON BOARD THE CX INSTRUMENT. NO INJURY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SYNCHRON® CX9 PRO CLINICAL SYSTEMS CLINICAL CHEMISTRY ANALYZER JJE BECKMAN COULTER INC. CX9 PRO N/A

Patients

Seq Age Sex Outcome Treatment
1