FDA Adverse Event Other Summary report: N

GUARDIAN WALKER

MDR report key: 412190 · Received August 22, 2002

Report

Report Number
2020334-2002-00007
Event Type
Other
Date Received
August 22, 2002
Report Date
August 22, 2002
Manufacturer
SUNRISE MEDICAL/PCP DIVISION
Product Code
ITJ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE END USER WAS USING THE WALKER AT HOME, WHEN THE WALKER COLLAPSED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GUARDIAN WALKER PATIENT WALKER ITJ SUNRISE MEDICAL/PCP DIVISION 30755P NA

Patients

Seq Age Sex Outcome Treatment
1 74 YR Hospitalization| O