FDA Adverse Event Injury Summary report: N

NATUS DISPOSABLE DISC ELECTRODES

MDR report key: 4929566 · Received July 21, 2015

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

Additional Manufacturer Narrative · 1

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).

Description of Event or Problem · 1

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