FDA Adverse Event
Malfunction
Summary report: N
GOLVO
MDR report key: 3173511
·
Received May 31, 2013
Report
- Report Number
- 8030916-2013-00029
- Event Type
- Malfunction
- Date Received
- May 31, 2013
- Manufacturer
- LIKO AB
- Product Code
- FSA
- Report Source
- Manufacturer report
Narratives
Description of Event or Problem · 1
(B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 241788 | GOLVO | NON-AC POWERED PATIENT LIFT | FSA | LIKO AB |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |