FDA Adverse Event Malfunction Summary report: N

QUICKIE 2 WHEELCHAIR

MDR report key: 189642 · Received September 30, 1998

Report

Report Number
2082643-1998-01256
Event Type
Malfunction
Date Received
September 30, 1998
Date of Event
September 30, 1998
Report Date
September 30, 1998
Manufacturer
SUNRISE MEDICAL MPD
Product Code
IOR
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
SERVICE PERSONNEL

Narratives

Description of Event or Problem · 1

RPTR CLAIMS X-TUBE BROKE AT THE SEAT TUBE WELD AREA WHILE CHAIR WAS IN USE. NO INJURIES INVOLVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 QUICKIE 2 WHEELCHAIR WHEELCHAIR, MECHANICAL IOR SUNRISE MEDICAL MPD NA P/N-672616

Patients

Seq Age Sex Outcome Treatment
1 48 YR Other