FDA Adverse Event Injury Summary report: N

PRIDE MOBILITY PRODUCTS

MDR report key: 2211952 · Received August 15, 2011

Report

Report Number
2530130-2011-00034
Event Type
Injury
Date Received
August 15, 2011
Date of Event
May 12, 2011
Report Date
August 11, 2011
Manufacturer
PRIDE MOBILITY PRODUCTS
Product Code
ITI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

DEVICE NOT AVAILABLE FOR EVALUATION. WILL SUBMIT A FOLLOW-UP INVESTIGATION REPORT SHOULD THE DEVICE BECOME AVAILABLE.

Description of Event or Problem · 1

THE END USER ALLEGES THAT HIS LOWER EXTREMITIES DO NOT PROPERLY FIT INTO FRONT RIGGINGS OF UNIT. REQUESTING STRAPS FROM DEALER. LEFT FOOT FELL OFF RIGGINGS AND SUSTAINED FOOT INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PRIDE MOBILITY PRODUCTS POWERED WHEELCHAIR ITI PRIDE MOBILITY PRODUCTS QUANTUM 600

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization