FDA Adverse Event Injury Summary report: N

UNK

MDR report key: 617658 · Received June 24, 2005

Report

Report Number
617658
Event Type
Injury
Date Received
June 24, 2005
Date of Event
May 27, 2005
Report Date
June 24, 2005
Manufacturer
UNK
Product Code
ETD
Report Source
User Facility report
Reporter Location
TX, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

REMOVAL OF L EAR TUBE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UNK UNK ETD UNK UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 3 YR Required Intervention