NATUS DISPOSABLE DISC ELECTRODES
Report
- Report Number
- 3010611950-2015-00005
- Event Type
- Injury
- Date Received
- July 21, 2015
- Date of Event
- June 30, 2015
- Report Date
- July 2, 2015
- Manufacturer
- NATUS NEUROLOGY, INCORPORTAED
- Product Code
- GXY
- PMA / PMN Number
- K850108
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MO, US
- Reporter Occupation
- NURSE
Narratives
1) REGISTERED INTERNALLY AS A COMPLAINT ((B)(4)) FOR FURTHER INVESTIGATION BY MANUFACTURER. 2) THE ELECTRODES DESCRIBED ARE MANUFACTURED FOR NATUS NEUROLOGY INC. BY A CONTRACT MANUFACTURER. 3) SAMPLES TAKEN FROM THE SAME LOT OF PRODUCT WERE EVALUATED BY THE CONTRACT MANUFACTURER AND FOUND TO MEET ALL MANUFACTURING SPECIFICATIONS. 4) A SEPARATE MDR HAS BEEN CREATED AND SUBMITTED FOR THE EQUIPMENT USED (REF MDR 3010611950-2015-00003). 5) ELECTRO-CAUTERY EQUIPMENT WAS IN USE BY THE COMPLAINANT AT THE SAME TIME AS THE NATUS DEVICE IN QUESTION. THERE ARE KNOWN RISKS ASSOCIATED WITH SUCH DEVICE TO DEVICE COMBINATIONS WHERE ELECTRODES CAN INTERCEPT STRAY RADIO FREQUENCY ENERGY AND RESULT IN THERMAL HEATING. NATUS SAFETY INFORMATION SUPPLIED TO END USERS STATES SUCH INTERACTIONS EXIST AND WARNS END USERS THAT ELECTRODE DISCONNECTION MAY BE NEEDED TO AVOID SUCH INTERACTIONS (REF NATUS SAFETY REFERENCE GUIDE, LABEL #269-594705).
PATIENT WAS BURNED DURING SPINAL FUSION AT THE SIDE OF STIMULATING ELECTRODES. PROCEDURE WAS 6 -- 7 HOURS. CUSTOMER WAS ALSO USING AN ELECTRO-CAUTERY INSTRUMENT (NOT A NATUS DEVICE).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 471204 | NATUS DISPOSABLE DISC ELECTRODES | ELECTRODE | GXY | NATUS NEUROLOGY, INCORPORTAED | 019-415000 | 406609 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 13 YR | Other |