FDA Adverse Event
Malfunction
Summary report: N
VIKING
MDR report key: 3233378
·
Received July 10, 2013
Report
- Report Number
- 8030916-2013-00044
- Event Type
- Malfunction
- Date Received
- July 10, 2013
- Manufacturer
- LIKO AB
- Product Code
- FSA
- Product Problem
- Yes
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
A SUPPLEMENTARY REPORT WILL BE FILED WHEN THE SLING BAR HAS BEEN RETURNED AND AN EVAL IS PERFORMED.
Description of Event or Problem · 1
(B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 315493 | VIKING | NON-AC POWERED PATIENT LIFT | FSA | LIKO AB |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |