FDA Adverse Event Other Summary report: N

PRIDE

MDR report key: 1790578 · Received August 2, 2010

Report

Report Number
2530130-2010-00042
Event Type
Other
Date Received
August 2, 2010
Date of Event
June 11, 2010
Report Date
July 28, 2010
Manufacturer
PRIDE MOBILITY PRODUCTS CORP.
Product Code
ITI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

DEVICE EVALUATION ANTICIPATED BUT NOT YET BEGUN. A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF INVESTIGATION.

Description of Event or Problem · 1

IT IS ALLEGED THAT THE CUSTOMER WAS TRANSFERRING WHEN THE SEAT ON HER POWERCHAIR BROKE, RESULTING IN A FALL REQUIRING AN ER VISIT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PRIDE POWERCHAIR ITI PRIDE MOBILITY PRODUCTS CORP. 1103 ULTRA NA

Patients

Seq Age Sex Outcome Treatment
1 UNK Hospitalization