FDA Adverse Event
Malfunction
Summary report: N
SABINA SLINGBAR
MDR report key: 1981139
·
Received January 31, 2011
Report
- Report Number
- 8030916-2011-00003
- Event Type
- Malfunction
- Date Received
- January 31, 2011
- Report Date
- December 21, 2010
- Manufacturer
- LIKO AB
- Product Code
- FNG
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- DA
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
(B)(4). RETROSPECTIVE REVIEW OF COMPLAINTS. THIS HAS BEEN DEEMED TO BE REPORTABLE.
Description of Event or Problem · 1
SLING BAR RETURNED TO MANUFACTURER UNDER SERVICE ORDER #70733. NO ALLEGATION OF INJURY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SABINA SLINGBAR | NON-AC POWERED PATIENT LIFT | FNG | LIKO AB | COMFORT SLINGBAR |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |