FDA Adverse Event
Summary report: N
ULTRA PRO
MDR report key: 1988359
·
Received February 4, 2011
Report
- Report Number
- 1988359
- Date Received
- February 4, 2011
- Date of Event
- January 26, 2011
- Report Date
- February 4, 2011
- Manufacturer
- BIODEX MEDICAL SYSTEMS INC.
- Product Code
- IXR
- Report Source
- User Facility report
- Reporter Location
- TN, US
Narratives
Description of Event or Problem · 1
FOLLOWING AN ULTRASOUND, THE PATIENT WAS SITTING AND PREPARING TO STAND UP. THE PATIENT WAS SLIDING DOWN TO THE FOOT OF THE TABLE WHEN THE FOOT SECTION DROPPED AND THE PATIENT FELL TO THE FLOOR IN A SITTING POSITION. THE PATIENT DID NOT SUSTAIN ANY INJURY. BIOMED WAS CALLED TO EXAMINE THE TABLE AND WAS NOT ABLE TO DUPLICATE THE FALL. IT IS POSSIBLE THAT THE PATIENT'S CLOTHING MAY HAVE BEEN CAUGHT ON THE RELEASE LATCH.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ULTRA PRO | ULTRASOUND TABLE | IXR | BIODEX MEDICAL SYSTEMS INC. | 058-720 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 71 YR | NO OTHER THERAPIES |