FDA Adverse Event Injury Summary report: N

CARDINAL HEALTH

MDR report key: 2212490 · Received January 4, 2008

Report

Report Number
2212490
Event Type
Injury
Date Received
January 4, 2008
Date of Event
December 30, 2007
Report Date
January 2, 2008
Product Code
KDQ
Report Source
User Facility report
Reporter Location
CA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

DURING A THORACENTESIS, SEVERAL INCHES OF TUBING WAS SHEARED OFF AND REMAINED IN THE PT. THIS REQUIRED SURGERY TO REMOVE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CARDINAL HEALTH THORACENTESIS TRAY KDQ

Patients

Seq Age Sex Outcome Treatment
1 79 YR Required Intervention