FDA Adverse Event
Malfunction
Summary report: N
NON AC-POWERED PATIENT LIFT
MDR report key: 3183138
·
Received June 21, 2013
Report
- Report Number
- 9616091-2013-01054
- Event Type
- Malfunction
- Date Received
- June 21, 2013
- Report Date
- May 28, 2013
- Manufacturer
- INVAMEX
- Product Code
- FSA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- OTHER CAREGIVERS
Narratives
Description of Event or Problem · 1
FACILITY STATES HANGER BAR WHERE THE SLING ATTACHES ALMOST DID A 360; WASN'T STEADY OR STABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 283371 | NON AC-POWERED PATIENT LIFT | 880.5510 | FSA | INVAMEX | RPL450-1 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |