FDA Adverse Event
Malfunction
Summary report: N
KODAK X-MATIC ID CAMERA
MDR report key: 263276
·
Received February 15, 2000
Report
- Report Number
- 1315356-2000-00001
- Event Type
- Malfunction
- Date Received
- February 15, 2000
- Date of Event
- January 17, 2000
- Report Date
- February 14, 2000
- Manufacturer
- EASTMAN KODAK CO.
- Product Code
- IZJ
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CT, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
TWO TECHNOLOGISTS RECEIVED SHOCKS FROM A NEWLY INSTALLED CAMERA. THE CAMERA AND ELECTRICAL OUTLET WAS SUBSEQUENTLY TESTED BY AN ELECTRICIAN. THE ELECTRICIAN INDICATED THAT THE TECHNOLOGIST WAS SHOCKED WITH 108 VOLTS. THE ELECTRICIAN BELIEVED THE DEVICE WAS NOT GROUNDED. THE SECOND ELECTRICIAN CONSULTED A CARDIOLOGIST. NO DAMAGE WAS NOTED BY AN EKG EVAL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | KODAK X-MATIC ID CAMERA | PATIENT ID CAMERA | IZJ | EASTMAN KODAK CO. | 2 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Life Threatening |