FDA Adverse Event
Summary report: N
KINAIR
MDR report key: 1032598
·
Received March 27, 2008
Report
- Report Number
- 1032598
- Date Received
- March 27, 2008
- Date of Event
- February 9, 2008
- Report Date
- March 27, 2008
- Manufacturer
- KINETIC CONCEPTS, INC.
- Product Code
- INX
- Report Source
- User Facility report
- Reporter Location
- MI, US
Narratives
Description of Event or Problem · 1
AS I WAS LEAVING ANOTHER PATIENT'S ROOM THE TECH SAID MY PATIENT WAS FOUND ON THE FLOOR. WIFE WAS AT BEDSIDE, PATIENT HAD BEEN AGITATED, MD HAD BEEN PAGED REGARDING IT. MD WAS PAGED AGAIN AND CAME TO BEDSIDE AFTER PATIENT WAS FOUND ON THE FLOOR. THE THREE SIDERAILS WERE UP HOWEVER PT SLID DOWN AT BOTTOM OF BED AND WAS FOUND ON FLOOR. AIR TUBE NEAR BOTTOM OF BED WAS NOT FULLY INFLATED AND HAD BEEN EARLIER BECAUSE THE TECH AND I HAD BEEN PULLING HIM UP IN THE BED WHEN HE'D SLIDE DOWN. FAULTY BED WAS REMOVED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | KINAIR | BED, HOSPITAL | INX | KINETIC CONCEPTS, INC. | KINAIR | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 62 YR |