FDA Adverse Event
Malfunction
Summary report: N
EVERET-JENNINGS WHEELCHAIR
MDR report key: 23905567
·
Received December 29, 2025
Report
- Report Number
- MW5181234
- 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 EVERETT-JENNINGS WHEELCHAIR, SERIAL NUMBER (B)(6) THAT HAD BRAKES THAT COULD NOT BE ENGAGED. 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 |
|---|---|---|---|---|---|---|---|
| 2600357 | EVERET-JENNINGS WHEELCHAIR | WHEELCHAIR, MECHANICAL | IOR | GF HEALTH PRODUCTS, INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |