FDA Adverse Event Malfunction Summary report: N

SYNCHRON LX CO2 ACID REAGENT

MDR report key: 2120606 · Received June 10, 2011

Report

Report Number
2050012-2011-02138
Event Type
Malfunction
Date Received
June 10, 2011
Date of Event
May 17, 2011
Report Date
May 17, 2011
Manufacturer
BECKMAN COULTER INC.
Product Code
JFL
PMA / PMN Number
K965240
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

REPLACEMENT REAGENT WAS SENT.

Description of Event or Problem · 1

A CUSTOMER CONTACTED BECKMAN COULTER INC., (BCI) AND REPORTED THAT THE CAP ON THE SYNCHRON LX CO2 ACID REAGENT BOTTLE WAS LOOSE. NO INJURY WAS REPORTED ON THIS ISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SYNCHRON LX CO2 ACID REAGENT CO2 ACID REAGENT JFL BECKMAN COULTER INC. NA Z103207

Patients

Seq Age Sex Outcome Treatment
1