FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3952545 · Received July 23, 2014

Report

Report Number
9616091-2014-01280
Event Type
Malfunction
Date Received
July 23, 2014
Report Date
June 18, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

TAC- (B)(6) 2014 - NO INJURY ALLEGED. MALFUNCTION ALLEGED. FRAME BENT/BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
431466 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX STDT422HD WHEELCHAIR

Patients

Seq Age Sex Outcome Treatment
1 Other