FDA Adverse Event Injury Summary report: N

PRIDE MOBILITY PRODUCTS

MDR report key: 23142456 · Received September 25, 2025

Report

Report Number
2530130-2025-00989
Event Type
Injury
Date Received
September 25, 2025
Date of Event
May 20, 2025
Report Date
September 25, 2025
Manufacturer
PRIDE MOBILITY PRODUCTS CORPORATION
Product Code
ITI
PMA / PMN Number
K042612
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

THE DEVICE HAS NOT YET BEEN MADE AVAILABLE FOR EVALUATION. SHOULD FURTHER INFORMATION OR THE DEVICE BECOME AVAILABLE, A FOLLOW-UP REPORT WILL THEN BE ISSUED.

Description of Event or Problem · 0

CONSUMER ALLEGES HIS FOOTPLATE ALLEGEDLY GOT LOOSE AND SHIMMIED DOWN. AS HE WAS GOING OUT THE BACK DOOR THE FOOTPLATE GOT CAUGHT AND ALLEGEDLY THREW HIM AND HIS UNIT DOWN TO THE BOTTOM OF THE RAMP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1850483 PRIDE MOBILITY PRODUCTS WHEELCHAIR, POWERED ITI PRIDE MOBILITY PRODUCTS CORPORATION J4 N/A

Patients

Seq Age Sex Outcome Treatment
1 NA Male Other