FDA Adverse Event
Injury
Summary report: N
ECG LIMB CLAMP ELECTRODES
MDR report key: 1070923
·
Received July 7, 2008
Report
- Report Number
- 1218950-2008-00381
- Event Type
- Injury
- Date Received
- July 7, 2008
- Report Date
- February 13, 2008
- Manufacturer
- AGILENT TECHNOLOGIES, INC
- Product Code
- DRX
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- HK
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE DEVCIE DOES NOT HAVE A SERIAL NUMBER; THEREFORE, THE MFG DATE CANNOT BE DETERMINED.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT THE PT RECEIVED A LACERATION FROM THE METAL PLATE OF THE ECG LIMB CLAMP ELECTRODE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ECG LIMB CLAMP ELECTRODES | ELECTRODE, ELECTROCARDIOGRAPH | DRX | AGILENT TECHNOLOGIES, INC | 40494E |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |