FDA Adverse Event
Summary report: N
DAILY ACTIVITY ASSIST DEVICES
MDR report key: 2921315
·
Received January 17, 2013
Report
- Report Number
- 1531186-2013-00240
- Date Received
- January 17, 2013
- Report Date
- January 17, 2013
- Manufacturer
- LERADO GLOBAL
- Product Code
- IKX
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Narratives
Description of Event or Problem · 1
ON (B)(6) -THE DEALER REPORTED THAT 980-4 COMMODE BACK BRACKET WAS BROKEN. THERE WAS NO PATIENT INJURY REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 26762 | DAILY ACTIVITY ASSIST DEVICES | 890.5050 | IKX | LERADO GLOBAL | 9830-4 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |