FDA Adverse Event Malfunction Summary report: N

EVEREST =-JENNINGS WHEELCHAIR

MDR report key: 23905461 · Received December 29, 2025

Report

Report Number
MW5181226
Event Type
Malfunction
Date Received
December 29, 2025
Report Date
December 18, 2025
Manufacturer
GF HEALTH PRODUCTS, INC.
Product Code
IOR
Product Problem
Yes
Report Source
Voluntary report
Reporter Occupation
UNKNOWN
Health Professional
*

Narratives

Description of Event or Problem · 0

STRYKER MEDICAL WAS NOTIFIED OF A POTENTIALLY REPORTABLE COMPLAINT INVOLVING A PRODUCT FOR WHICH STRYKER IS NOT THE ORIGINAL EQUIPMENT MANUFACTURER OF THE REPORTED DEVICE. THE CUSTOMER ALLEGED A MANUFACTURER EVEREST-JENNINGS WHEELCHAIR, SERIAL NUMBER UNKNOWN THAT HAD INOPERATE STIR-UPS AND REDUCED BRAKE FORCE. PLEASE FIND ADDITIONAL CONTACT INFORMATION BELOW. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1892324 EVEREST =-JENNINGS WHEELCHAIR WHEELCHAIR, MECHANICAL IOR GF HEALTH PRODUCTS, INC.

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown