FDA Adverse Event
Summary report: N
CLINITRON RITE-HITE P0100010019
MDR report key: 376165
·
Received February 8, 2002
Report
- Report Number
- 1045510-2002-00001
- Date Received
- February 8, 2002
- Date of Event
- January 19, 2002
- Report Date
- January 23, 2002
- Manufacturer
- HILL-ROM MANUFACTURING, , INC.
- Product Code
- INX
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- INVALID DATA
Narratives
Description of Event or Problem · 1
AS STATED BY NURSE, PT HAD BEEN PLACED IN SIDELYING POSITION BY NURSE PRIOR TO AM CLEANING OF PT. NURSE WENT INTO RESTROOM TO PREPARE LINENS. IT WAS WAS STATED THAT THEY BELIEVE BEADS ACCUMULATED BEHIND PT'S BUTTOCKS AND INERTIA CAUSED PT TO FALL OUT OF BED. PT SUFFERED A BRUISE ON HIP AND IT WAS NOT FOUND UNTIL TWO DAYS LATER THAT PT ALSO HAD A BROKEN COLLAR BONE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CLINITRON RITE-HITE P0100010019 | THERAPY | INX | HILL-ROM MANUFACTURING, , INC. | P0100010019 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Other |