FDA Adverse Event
Malfunction
Summary report: N
MECHANICAL (MANUAL) WHEELCHAIR
MDR report key: 3903247
·
Received June 30, 2014
Report
- Report Number
- 9616091-2014-01103
- Event Type
- Malfunction
- Date Received
- June 30, 2014
- Report Date
- May 28, 2014
- Manufacturer
- INVAMEX
- Product Code
- IOR
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IA, US
- Reporter Occupation
- MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Narratives
Description of Event or Problem · 1
DEALER ALLEGED THAT THE CASTER WHEELS ARE FLEXED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 380111 | MECHANICAL (MANUAL) WHEELCHAIR | 890.3850 | IOR | INVAMEX | SL2028F |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |