FDA Adverse Event Injury Summary report: N

HEMI-WALKER

MDR report key: 84875 · Received April 18, 1997

Report

Report Number
MW1011154
Event Type
Injury
Date Received
April 18, 1997
Date of Event
April 13, 1997
Report Date
April 16, 1997
Manufacturer
DURO-MED INDUSTRIES, INC.
Product Code
ITJ
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
FL, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PT WAS SITTING ON BSC LEANING FORWARD, LOST BALANCE. LEANED RIGHT ONTO HEMI WALKER. LEG OF WALKER BROKE, PT FELL. SUSTAINED FX (L) RING FINGER. SWELLING AND BRUISING TO INJURED AREA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HEMI-WALKER WALKER ITJ DURO-MED INDUSTRIES, INC. 1306 *

Patients

Seq Age Sex Outcome Treatment
1 67 YR Required Intervention