FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3252817 · Received July 29, 2013

Report

Report Number
1531186-2013-03443
Date Received
July 29, 2013
Report Date
July 11, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES LEFT REAR CASTER IS SHOT. PN 1151018.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
353655 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65350GR

Patients

Seq Age Sex Outcome Treatment
1 Other