FDA Adverse Event
Malfunction
Summary report: N
GOLVO
MDR report key: 3130459
·
Received March 26, 2013
Report
- Report Number
- 8030916-2013-00019
- Event Type
- Malfunction
- Date Received
- March 26, 2013
- Manufacturer
- LIKO AB
- Product Code
- FSA
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
THIS IS AN INITIAL REPORT. A SUPPLEMENTARY REPORT WILL BE FILED AS SOON AS THE DEFECTIVE PARTS HAS BEEN RETURNED TO THE MANUFACTURER FOR EVALUATION.
Description of Event or Problem · 1
REFERENCE TO IMPORTER REPORT # (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 125409 | GOLVO | NON-AC POWERED PATIENT LIFT | FSA | LIKO AB |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |