FDA Adverse Event
Malfunction
Summary report: N
ALCO WHEELCHAIR
MDR report key: 23905564
·
Received December 29, 2025
Report
- Report Number
- MW5181233
- Event Type
- Malfunction
- Date Received
- December 29, 2025
- Report Date
- December 18, 2025
- Manufacturer
- ALCO SALES & SERVICE CO.
- Product Code
- IOR
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Occupation
- UNKNOWN
- Health Professional
- *
Narratives
Description of Event or Problem · 0
(B)(6) WAS NOTIFIED OF A POTENTIALLY REPORTABLE COMPLAINT INVOLVING A PRODUCT FOR WHICH (B)(6) IS NOT THE ORIGINAL EQUIPMENT MANUFACTURER OF THE REPORTED DEVICE. THE CUSTOMER ALLEGED A MANUFACTURER ALCO 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).
Description of Event or Problem · 0
ADDITIONAL INFORMATION RECEIVED ON 01/23 FOR MW5181233 TO UPDATE MANUFACTURER TO ALCO SALES & SERVICE CO. AND PROCODE TO IOR.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2600354 | ALCO WHEELCHAIR | WHEELCHAIR, MECHANICAL | IOR | ALCO SALES & SERVICE CO. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |