FDA Adverse Event
Other
Summary report: N
GULDMANN MOBILE HOIST
MDR report key: 748487
·
Received August 3, 2005
Report
- Report Number
- MW1036247
- Event Type
- Other
- Date Received
- August 3, 2005
- Date of Event
- July 15, 2005
- Report Date
- July 25, 2005
- Manufacturer
- V-GULDMANN A/S
- Product Code
- FSA
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- KS, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
RESIDENT WAS BEING TRANSFERRED VIA LIFT, OUR STREP CAME UNHOOKED AND RESIDENT FELL TO FLOOR.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GULDMANN MOBILE HOIST | MOBILE HOIST | FSA | V-GULDMANN A/S | 21-XXX-4793 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 84 YR | Other |