FDA Adverse Event Injury Summary report: N

ALLEN MEDICAL SYSTEMS

MDR report key: 358334 · Received October 25, 2001

Report

Report Number
MW1023208
Event Type
Injury
Date Received
October 25, 2001
Date of Event
January 5, 2000
Report Date
October 25, 2001
Manufacturer
ALLEN MEDICAL SYSTEMS
Product Code
EYD
Report Source
Voluntary report
Reporter Location
VA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PT WAS IN OPERATING ROOM. THE HYDRAULIC STIRUP WAS LAYING ON THE FLOOR. WHEN PT WAS INSTALLING ON TABLE, LEFT RING AND INDEX FINGERS GOT CAUGHT IN THE UPPER PORTION OF THE STIRUP. THE STIRUP COULD NOT BE REMOVED EASILY, SO PT WAS TAKEN TO THE EMERGENCY ROOM. THE STIRUP WAS REMOVED AND PT WAS SENT FOR PHYSICAL THERAPY FOLLOW-UP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
47960 ALLEN MEDICAL SYSTEMS GYN STIRRUP EYD ALLEN MEDICAL SYSTEMS 10023 *

Patients

Seq Age Sex Outcome Treatment
1 42 YR Other| R