FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3103308 · Received May 9, 2013

Report

Report Number
1531186-2013-01971
Date Received
May 9, 2013
Date of Event
March 5, 2013
Report Date
April 12, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NM, US
Reporter Occupation
PATIENT FAMILY MEMBER OR FRIEND

Narratives

Description of Event or Problem · 1

ALLEGEDLY BRAKES BROKE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
204367 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65650

Patients

Seq Age Sex Outcome Treatment
1 Other