FDA Adverse Event
Summary report: N
GH3 LIFT
MDR report key: 3341086
·
Received July 29, 2013
Report
- Report Number
- 3341086
- Date Received
- July 29, 2013
- Date of Event
- July 20, 2013
- Report Date
- July 29, 2013
- Manufacturer
- GULDMANN, INC.
- Product Code
- FNG
- Report Source
- User Facility report
- Reporter Location
- PA, US
- Reporter Occupation
- INVALID DATA
Narratives
Description of Event or Problem · 1
MOVING PATIENT USING LIFT DEVICE IN ROOM AS LIFT WAS IN DOWN POSITION WOULD NOT MOVE UP. AN ORANGE LIGHT ON THE MACHINE WAS ENGAGE AND THEN THE DEVICE WOULD NOT LIFT THE PATIENT UP. RESET BUTTON WAS PUSHED TO ASSIST BUT DID NOTHING TO CORRECT THE ISSUE. EMERGENCY RELEASE WAS PULLED AND PATIENT WAS SAFELY LOWERED USING MULTIPLE STAFF TO ASSIST.MANUFACTURER RESPONSE FOR PATIENT LIFT, GULDMANN GH3 CEILING LIFT SYSTEM (PER SITE REPORTER).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 354913 | GH3 LIFT | LIFT, PATIENT, AC-POWERED | FNG | GULDMANN, INC. | GH3 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 89 YR |