FDA Adverse Event Malfunction Summary report: N

1CC E-TB SYR 25X5/8

MDR report key: 417017 · Received September 9, 2002

Report

Report Number
1915484-2002-00015
Event Type
Malfunction
Date Received
September 9, 2002
Date of Event
August 16, 2002
Report Date
September 6, 2002
Manufacturer
TYCOHEALTHCARE/KENDALL
Product Code
FMF
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

A CUSTOMER HAD SUSTAINED A CLEAN NEEDLESTICK. THE CUSTOMER STATED THAT AN EMPLOYEE WAS STUCK BY A NEEDLE THAT WAS STICKING OUT OF THE PACKAGING BECAUSE THERE WAS NO CAP ON THE NEEDLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 1CC E-TB SYR 25X5/8 TB SYRINGE FMF TYCOHEALTHCARE/KENDALL * 131003

Patients

Seq Age Sex Outcome Treatment
1 * Other