FDA Adverse Event Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3961859 · Received July 28, 2014

Report

Report Number
1531186-2014-02815
Date Received
July 28, 2014
Report Date
June 23, 2014
Manufacturer
UNKNOWN
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES THAT THE (B)(4) FOOTREST THEY ORDER FOR THEIR VERANDA STANDARD WHEELCHAIR WILL HOOK ON THE CHAIR BUT WILL NOT LOCK INTO PLACE. PROVIDER DID NOT SPECIFY HOW MANY TIMES THIS HAPPENED. PROVIDER ADVISED ACCORDING TO OUR INFORMATION THESE TWO MODEL SHOULD BE COMPATIBLE BUT THEY ARE NOT FROM THEIR EXPERIENCE. NO ADDITIONAL INFORMATION PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
439735 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN V18RFR

Patients

Seq Age Sex Outcome Treatment
1 Other