FDA Adverse Event
Malfunction
Summary report: N
WHEELCHAIR ACCESSORY
MDR report key: 3230164
·
Received July 16, 2013
Report
- Report Number
- 9616091-2013-01228
- Event Type
- Malfunction
- Date Received
- July 16, 2013
- Report Date
- June 26, 2013
- Manufacturer
- INVAMEX
- Product Code
- KNO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OK, US
- Reporter Occupation
- MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Narratives
Description of Event or Problem · 1
THE PROVIDER STATED THE LEVER AND THE FOOTPLATE HAVE ALL BROKEN ON THESE LEGRESTS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 329966 | WHEELCHAIR ACCESSORY | 890.3910 | KNO | INVAMEX | T94HC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |