FDA Adverse Event
Injury
Summary report: N
HISPEED NX/I
MDR report key: 772377
·
Received October 23, 2006
Report
- Report Number
- 2126677-2006-00022
- Event Type
- Injury
- Date Received
- October 23, 2006
- Date of Event
- September 24, 2006
- Report Date
- October 23, 2006
- Manufacturer
- GE YOKOGAWA MEDICAL SYSTEMS
- Product Code
- JAK
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT, A NURSE INJURED A FINGER TENDON WHEN SHE PLACED HER FINGER IN A GAP BETWEEN THE CRADLE AND THE COVER. THE HCP MOVED THE CRADLE BACKWARDS UNAWARE THAT THE NURSE'S HAND WAS ON THE TABLE. NO LACERATIONS WERE REPORTED. A SPLINT MAY HAVE BEEN NECESSARY FOR A FEW DAYS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HISPEED NX/I | CT | JAK | GE YOKOGAWA MEDICAL SYSTEMS | 2113694 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 22 YR | Required Intervention |