FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3253185 · Received July 29, 2013

Report

Report Number
1525712-2013-06273
Event Type
Malfunction
Date Received
July 29, 2013
Report Date
July 10, 2013
Manufacturer
UNKNOWN
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PROVIDER STATES BOTH THE LEFT AND RIGHT FOOT PLATES ARE CRACKED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
352787 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN TRSX5

Patients

Seq Age Sex Outcome Treatment
1 Other