FDA Adverse Event Injury Summary report: N

PRIDE MOBILITY PRODUCTS

MDR report key: 2873847 · Received December 14, 2012

Report

Report Number
2530130-2012-00085
Event Type
Injury
Date Received
December 14, 2012
Date of Event
November 19, 2012
Report Date
June 20, 2013
Manufacturer
PRIDE MOBILITY PRODUCTS
Product Code
ITI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE IS NOT AVAILABLE FOR EVALUATION BY PRIDE AT THIS TIME. SHOULD THE DEVICE OR FURTHER INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL THEN BE SUBMITTED.

Additional Manufacturer Narrative · 1

THE DEVICE WAS RETURNED AND EVALUATED. THE ALLEGED INADVERTENT MOVEMENT COULD NOT BE DUPLICATED. THE NATURE OF THE COMPLAINT IS UNKNOWN.

Description of Event or Problem · 1

DEALER CLAIMS CONSUMER WAS ON THE SIDEWALK GOING UP A HILL WHEN ALLEGEDLY THE PWC TOOK AN IMMEDIATE RIGHT AND WENT UP A DIRT HILL.

Description of Event or Problem · 1

DEALER CLAIMS CONSUMER WAS ON THE SIDEWALK GOING UP A HILL WHEN ALLEGEDLY THE PWC TOOK AN IMMEDIATE RIGHT AND WENT UP A DIRT HILL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PRIDE MOBILITY PRODUCTS POWERED WHEELCHAIR ITI PRIDE MOBILITY PRODUCTS Q600

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization