FDA Adverse Event Other Summary report: N

QUICKIE

MDR report key: 1062840 · Received June 17, 2008

Report

Report Number
2937137-2008-00007
Event Type
Other
Date Received
June 17, 2008
Date of Event
May 19, 2008
Report Date
June 17, 2008
Manufacturer
SUNRISE MEDICAL, INC.
Product Code
IOR
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

AS OF THIS DATE, THIS ITEM HAS NOT BEEN RETURNED TO THE MANUFACTURE FOR EVAL.

Description of Event or Problem · 1

THE REPORTER STATED THAT THE END-USER WAS WITH SOME FRIENDS, A FRIEND WAS PUSHING THE END-USER DOWN, AND INCLINE AT A FAST SPEED WHEN THE CHAIR RAN INTO A CRACK IN THE SIDEWALK, CAUSING THE CHAIR TO COME TO A QUICK STOP, THE END-USER'S FRIEND THAT WAS PUSHING THE END-USER, HIS MOMENTUM PUSHED THE CHAIR FORWARD CAUSING THE END-USER TO FALL. THERE WERE NO INJURIES TO THE END USER AS INITIALLY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 QUICKIE WHEELCHAIR, MECHANICAL IOR SUNRISE MEDICAL, INC. QUICKIE TITANIUM P/N EIT3

Patients

Seq Age Sex Outcome Treatment
1 Other