FDA Adverse Event
Malfunction
Summary report: N
VIKING M
MDR report key: 3841288
·
Received May 16, 2014
Report
- Report Number
- 8030916-2014-00036
- Event Type
- Malfunction
- Date Received
- May 16, 2014
- 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 |
|---|---|---|---|---|---|---|---|
| 293490 | VIKING M | NON-AC POWERED PATIENT LIFT | FSA | LIKO AB |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |