FDA Adverse Event Summary report: N

KENDALL 2 GA H-DROP TRNS YEL W/UNWND20

MDR report key: 638691 · Received September 30, 2005

Report

Report Number
1424643-2005-00010
Date Received
September 30, 2005
Report Date
September 26, 2005
Manufacturer
TYCO HEALTHCARE/KENDALL
Product Code
JKA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED TO TYCO HEALTHCARE KENDALL IN 2005 THAT A CUSTOMER HAD A PROBLEM WITH A SHARPS CONTAINER. ACCORDING TO THE CUSTOMER THERE WAS A NEEDLE STICK INJURY THAT OCCURRED IN JUNE. THE NURSE STUCK THEIR HANDS IN THE CONTAINER TO TRY AND GET MORENEEDLES INTO THE CONTAINER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 KENDALL 2 GA H-DROP TRNS YEL W/UNWND20 SHARPS CONTAINER JKA TYCO HEALTHCARE/KENDALL UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other