FDA Adverse Event Malfunction Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 4121763 · Received September 26, 2014

Report

Report Number
1525712-2014-06350
Event Type
Malfunction
Date Received
September 26, 2014
Date of Event
August 25, 2014
Report Date
September 4, 2014
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Description of Event or Problem · 1

NURSE ADVISED BOTH BRAKES DO NOT APPLY TO THE WHEELS 100 PERCENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
602169 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN SELFCARE

Patients

Seq Age Sex Outcome Treatment
1 Other