FDA Adverse Event Injury Summary report: N

CRAWFORD

MDR report key: 284453 · Received June 30, 2000

Report

Report Number
284453
Event Type
Injury
Date Received
June 30, 2000
Date of Event
June 23, 2000
Report Date
June 27, 2000
Manufacturer
WALSH MANUFACTURING LTD.
Product Code
HNW
Adverse Event
Yes
Product Problem
Yes
Report Source
User Facility report
Reporter Location
IL, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

THIS IS A PT WHO UNDERWENT A DACRYOCYSTORHINOSTOMY ON THE RIGHT SIDE. A LACRIMAL INTUBATION SET WAS USED AND ABOUT HALF OF THE WIRE BROKE OFF AND REMAINED IN THE PT'S NOSTRIL. THE PT WILL RETURN TO SURGERY IN 10 DAYS FOR REMOVAL OF FOREIGN BODY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CRAWFORD LACRIMAL INTUBATION SET HNW WALSH MANUFACTURING LTD. * *

Patients

Seq Age Sex Outcome Treatment
1 88 YR Required Intervention