FDA Adverse Event
Summary report: N
KINAIRE MED SURG
MDR report key: 1221104
·
Received October 15, 2008
Report
- Report Number
- 1221104
- Date Received
- October 15, 2008
- Date of Event
- October 9, 2008
- Report Date
- October 15, 2008
- Manufacturer
- KINETIC CONCEPTS, INC.
- Product Code
- INX
- Report Source
- User Facility report
- Reporter Location
- MN, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
PATIENT WAS AWAKE/ORIENTED AND SITTING UP IN THE KINAIRE SPECIALITY BED EATING LUNCH. THE PATIENT SLID DOWN THE SIDE OF THE BED AND ON TO THE FLOOR. (TWO SIDERAILS WERE UP.) THE PATIENT TOLD SPOUSE AND THE NURSE THAT THE MATTRESS IS TOO SLIPPERY AND THIS IS WHAT CONTRIBUTED TO THE FALL. THE PATIENT DID NOT HAVE ANY INJURIES. THE KINAIRE BED WAS DISCONTINUED AND A REGULAR BED WAS USED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | KINAIRE MED SURG | BED, LOW AIR LOSS | INX | KINETIC CONCEPTS, INC. | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 42 YR |