FDA Adverse Event
Other
Summary report: N
*
MDR report key: 1206683
·
Received October 15, 2008
Report
- Report Number
- 8030916-2008-00034
- Event Type
- Other
- Date Received
- October 15, 2008
- Manufacturer
- LIKO AB
- Product Code
- FSA
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
TO BE ABLE TO DETERMINE WHAT CAUSED THIS EVENT, WE WOULD NEED MORE SPECIFIC INFO REGARDING HOW "THE STRAP GOT STUCK". HOWEVER, IN OUR EXPERIENCE, JAMMING OF THE STRAP DOES NOT OCCUR WHEN THE LIFT IS USED PROPERLY ACCORDING TO MFR INSTRUCTIONS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | * | * | FSA | LIKO AB | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |