FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2524557 · Received April 10, 2012

Report

Report Number
1531186-2012-00118
Date Received
April 10, 2012
Report Date
April 9, 2012
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

CUSTOMER ALLEGED CRACKED AT BOTTOM OF H. NO INJURY ALLEGED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 6291-JR

Patients

Seq Age Sex Outcome Treatment
1 Other