FDA Adverse Event Malfunction Summary report: N

UNICEL® DXH 800 COULTER® CELLULAR ANALYSIS SYSTEM

MDR report key: 2242306 · Received September 10, 2011

Report

Report Number
1061932-2011-01434
Event Type
Malfunction
Date Received
September 10, 2011
Date of Event
August 11, 2011
Report Date
August 11, 2011
Manufacturer
BECKMAN COULTER INC.
Product Code
GKZ
PMA / PMN Number
K081930
Removal / Correction Number
N/A
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

NO SERVICE WAS REQUESTED FOR THIS EVENT. THE CUSTOMER STATED THAT THE SPILL OCCURRED BECAUSE THE DRAIN WHERE THE INSTRUMENTS WASTE TUBES ARE CONNECTED BECAME CLOGGED AND CAUSED THE WASTE TO BACKWASH AND SPILL. THE CUSTOMER RESOLVED THE ISSUE BY UNCLOGGING THE DRAIN. ROOT CAUSE FOR THE LEAK WAS THAT THE DRAIN WHERE THE WASTE TUBING IS CONNECTED WAS CLOGGED. BEC INTERNAL IDENTIFICATION NUMBER IS (B)(4).

Description of Event or Problem · 1

THE CUSTOMER CONTACTED BECKMAN COULTER INC (BEC) TO REPORT FINDING WASTE RESIDUE ON THE FLOOR, WALL, & DRAIN CAP WHERE THE WASTE LINES FOR TWO* DXH800 INSTRUMENTS ARE CONNECTED TO THE DRAIN. THE USER WAS WEARING PERSONAL PROTECTIVE EQUIPMENT (PPE) CONSISTING OF GOWN, GLOVES AND EYE GOGGLES AT THE TIME OF THE INCIDENT. THE MATERIAL SAFETY DATA SHEET (MSDS) WAS NOT REVIEWED; HOWEVER, IT IS READILY AVAILABLE. NO INJURIES OCCURRED AND MEDICAL ATTENTION WAS NOT SOUGHT. NO REPORTS OF EXPOSURE TO MUCOUS MEMBRANES OR OPEN WOUNDS. THE LAB'S EXPOSURE CONTROL OR RISK MANAGEMENT PLANS ARE IN PLACE. THE OTHER INSTRUMENT EVENT HAS BEEN CAPTURED UNDER MDR 1061932-2011-01436

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UNICEL® DXH 800 COULTER® CELLULAR ANALYSIS SYSTEM AUTOMATED DIFFERENTIAL CELL COUNTER GKZ BECKMAN COULTER INC. DXH800 N/A

Patients

Seq Age Sex Outcome Treatment
1