FDA Adverse Event
Malfunction
Summary report: N
NON AC-POWERED PATIENT LIFT
MDR report key: 3230603
·
Received July 16, 2013
Report
- Report Number
- 1525712-2013-05839
- Event Type
- Malfunction
- Date Received
- July 16, 2013
- Report Date
- June 26, 2013
- Manufacturer
- UNKNOWN
- Product Code
- FSA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- PATIENT
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT A 9805P HYDRAULIC LIFT LOWERS IMPROPERLY WITH WEIGHT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 328161 | NON AC-POWERED PATIENT LIFT | 880.5510 | FSA | UNKNOWN | 9805P |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |