FDA Adverse Event Summary report: N

HOSPIRA

MDR report key: 1183323 · Received September 22, 2008

Report

Report Number
1183323
Date Received
September 22, 2008
Date of Event
September 14, 2008
Report Date
September 22, 2008
Manufacturer
HOSPIRA GLOBAL MEDICAL AFFAIRS
Product Code
FPA
Report Source
User Facility report
Reporter Location
RI, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

A PRIMARY IV TUBING WAS RUNNING. NURSE WENT TO HANG A SECONDARY SET WITH A CHEMOTHERAPY AGENT THAT WAS RECEIVED FROM THE PHARMACY. NURSE CLAMPED THE PRIMARY SET WITH CLAMP PROVIDED ON THE SECONDARY SET, AND IT CUT THE PRIMARY TUBING COMPLETELY. NO CHEMO SPILL; NO HARM TO PT OR NURSE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HOSPIRA TUBING SET FPA HOSPIRA GLOBAL MEDICAL AFFAIRS NOT KNOWN NOT KNOWN

Patients

Seq Age Sex Outcome Treatment
1 *