FDA Adverse Event Malfunction Summary report: N

9XT SWINGAWAY FRAME STYLE 9153629153

MDR report key: 4912353 · Received July 14, 2015

Report

Report Number
9616091-2015-01827
Event Type
Malfunction
Date Received
July 14, 2015
Report Date
June 19, 2015
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

A FOLLOW UP WILL BE SENT IF THE PRODUCT OR ADDITIONAL INFORMATION IS OBTAINED.

Description of Event or Problem · 1

DEALER STATES THE RIGHT FRONT FRAME IS BENT BY THE HINGE PINS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
454921 9XT SWINGAWAY FRAME STYLE 9153629153 WHEELCHAIR, MECHANICAL IOR INVAMEX 9XT

Patients

Seq Age Sex Outcome Treatment
1 Other