FDA Adverse Event Injury Summary report: N

UNK

MDR report key: 117554 · Received August 22, 1997

Report

Report Number
117554
Event Type
Injury
Date Received
August 22, 1997
Date of Event
June 2, 1997
Report Date
July 25, 1997
Manufacturer
UNK
Product Code
JDN
Product Problem
Yes
Report Source
User Facility report
Reporter Location
IL, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

BROKEN SCREWS REMOVED FROM SPINAL AREA DUE TO INFECTION AND PSEUDARTHROSIS.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 47 YR Hospitalization| R