FDA Adverse Event
Malfunction
Summary report: N
VIKING
MDR report key: 3173442
·
Received June 4, 2013
Report
- Report Number
- 8030916-2013-00030
- Event Type
- Malfunction
- Date Received
- June 4, 2013
- Manufacturer
- LIKO AB
- Product Code
- FSA
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
A SUPPLEMENTARY REPORT WILL BE FILED WHEN THE FAILED PART IS RETURNED.
Description of Event or Problem · 1
(B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 247539 | VIKING | NON-AC POWERED PATIENT LIFT | FSA | LIKO AB |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |