FDA Adverse Event
Summary report: N
NICOLET LTM
MDR report key: 1805316
·
Received August 11, 2010
Report
- Report Number
- 1805316
- Date Received
- August 11, 2010
- Date of Event
- July 29, 2010
- Report Date
- August 11, 2010
- Manufacturer
- CAREFUSION 209 INC.
- Product Code
- GWQ
- Report Source
- User Facility report
- Reporter Location
- AR, US
Narratives
Description of Event or Problem · 1
WHEN AN EEG TECHNICIAN WAS MOVING A MOBILE EEG DEVICE TO DO A PATIENT STUDY, WHILE GETTING ON THE ELEVATOR, THE DEVICE TIPPED OVER ON THE TECHNICIAN AND CAUSED HER TO FALL AND INJURE HER HAND. STAFF MEMBER WAS SEEN IN THE ER. NO BROKEN BONES BUT BRUISING AND MEDICATION WAS PRESCRIBED.====================== HEALTH PROFESSIONAL'S IMPRESSION======================THESE NEWLY PURCHASED MOBILE LTM (LONG TERM MONITORING)EEG MACHINES ON A STAND ARE VERY TOP HEAVY IF ROLLED BACKWARDS.====================== MANUFACTURER RESPONSE FOR ELECTROENCEPHALOGRAPH, LTM======================THE MANUFACTURE STATES THEY WILL WORK WITH THEIR ENGINEERING TEAM TO EVALUATE THIS ISSUE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | NICOLET LTM | ELECTROENCEPHALOGRAPH | GWQ | CAREFUSION 209 INC. | LTM | N/A |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |