FDA Adverse Event Injury Summary report: N

INNOVATIVE PRODUCTS UNLIMITED, INC.

MDR report key: 705899 · Received April 25, 2006

Report

Report Number
1833497-2006-00003
Event Type
Injury
Date Received
April 25, 2006
Date of Event
March 10, 2006
Report Date
March 27, 2006
Manufacturer
INNOVATIVE PRODUCTS UNLIMITED, INC.
Product Code
INM
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

RESIDENT FELL OVER SIDEWAYS IN THE WALKER AND HIT HIS HEAD ON A DOOR KNOB. RESIDENT APPARENTLY WAS BLIND IN ONE EYE AND ALWAYS USED WALKER SOMEWHAT TURNED TOWARDS THE SIDE, MEANING BOTH HANDS WERE ALWAYS ON THE SAMW RAIL. RESIDENT SENT TO HOSPITAL AND EXPIRED IN 2006.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INNOVATIVE PRODUCTS UNLIMITED, INC. WALKER INM INNOVATIVE PRODUCTS UNLIMITED, INC. UNK *

Patients

Seq Age Sex Outcome Treatment
1 84 YR Hospitalization