FDA Adverse Event Summary report: N

1 QT N/S CONTAINER RED 100

MDR report key: 494631 · Received November 11, 2003

Report

Report Number
1424643-2003-00011
Date Received
November 11, 2003
Date of Event
October 21, 2003
Report Date
November 11, 2003
Manufacturer
TYCO HEALTHCARE/KENDALL
Product Code
MMK
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
INVALID DATA

Narratives

Description of Event or Problem · 1

A CUSTOMER HAD A PROBLEM WITH A SHARPS CONTAINER. THE CUSTOMER STATES THE NEEDLE PUNCTURED THE SIDE OF CONTAINER AND STUCK THE NURSE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 1 QT N/S CONTAINER RED 100 SHARPS CONTAINER MMK TYCO HEALTHCARE/KENDALL * 694393001791

Patients

Seq Age Sex Outcome Treatment
1 * Other