FDA Adverse Event
Other
Summary report: N
SPECIALITE
MDR report key: 408846
·
Received July 31, 2002
Report
- Report Number
- 1836145-2002-00010
- Event Type
- Other
- Date Received
- July 31, 2002
- Manufacturer
- HILL-ROM ARCHITECTURAL PRODUCTS HILL-ROM CO. INC.
- Product Code
- KZF
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
07/2002 CUSTOMER ALLEGES THAT ONE OF THEIR NURSES WAS ADJUSTING THE LIGHT WHEN NURSE FELT AN ELECTRICAL JOLT. THE NURSE WAS NOT INJURED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SPECIALITE | EXAM LIGHT | KZF | HILL-ROM ARCHITECTURAL PRODUCTS HILL-ROM CO. INC. | P645 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Other |