FDA Adverse Event Malfunction Summary report: N

HI PWR DISPOSBL GRNDING PAD

MDR report key: 1014067 · Received March 13, 2008

Report

Report Number
1717344-2008-00088
Event Type
Malfunction
Date Received
March 13, 2008
Date of Event
February 1, 2008
Report Date
February 12, 2008
Manufacturer
COVIDIEN LP (VALLEYLAB)
Product Code
ODR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DGPHP SITE BURNS CAN BE THE RESULT OF A NUMBER OF CAUSES INCLUDING PLACEMENT, DURATION OF TREATMENT AND POWER SETTINGS, PT CONDITION, AND POTENTIALLY BY FAILURE OF THE DISPERSIVE ELECTRODE TO PERFORM AS INTENDED. IN THIS CASE, WITHOUT THE RETURN OF THE INCIDENT DISPERSIVE ELECTRODE, WE WERE UNABLE TO DETERMINE IF ANY DEFECT OF THE PRODUCT CAUSED OR CONTRIBUTED TO THE INCIDENT. ONE OF THE CAUSES OF BURNS IS POOR DGPHP PLACEMENT. AS NOTED ABOVE, PROPER PLACEMENT OF THE DGPHP AND ENSURING GOOD CONTACT THROUGHOUT THE PROCEDURE (ESPECIALLY IF THE PT IS REPOSITIONED) ARE CRITICAL COMPONENTS TO AVOIDING BURNS. THIS IS COVERED IN DETAIL IN OUR IFU. FURTHERMORE, WE ARE AWARE THAT SOME CUSTOMERS REUSE PADS EVEN THOUGH THEY ARE CLEARLY LABELED AS SINGLE USE DEVICES. REUSED DISPERSIVE ELECTRODES CAN DRY OUT AND BE A SOURCE FOR BURNS BECAUSE THEY DO NOT CONDUCT ELECTRICAL CURRENT PROPERLY. WE ARE CLOSELY MONITORING THE INCIDENT RATE OF DISPERSIVE ELECTRODE BURNS. THE RATE OF BURNS FOR VALLEYLAB DGPHP DISPERSIVE ELECTRODES CONTINUES TO BE LOWER THAN THE OVERALL RATE OF RADIO FREQUENCY ABLATION DISPERSIVE ELECTRODE BURNS AS SITED IN CURRENT MEDICAL LITERATURE. CONTINUOUS IMPROVEMENT EFFORTS ARE ON-GOING TO ENSURE THAT CUSTOMERS ARE PROPERLY TRAINED AND OUR IFU CLEARLY ILLUSTRATES THE PROPER PLACEMENT OF THE DISPERSIVE ELECTRODES. WE ALSO REINFORCE THE IMPORTANCE OF NOT REUSING THESE SINGLE USE DEVICES TO THE CUSTOMER WHENEVER THE OPPORTUNITY ARISES.

Description of Event or Problem · 1

THE REPORT STATED THAT AFTER A RADIO FREQUENCY ABLATION PROCEDURE, THE PT'S SKIN REDDENED SLIGHTLY. THE PT EXPERIENCED NO PAIN. IT WAS ALSO NOTICED THAT THE ALUMINUM FILM ON THE PAD IS DISCOLORED. PT IS OK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HI PWR DISPOSBL GRNDING PAD ELECTROSURGICAL ACCESSORY ODR COVIDIEN LP (VALLEYLAB) UNK

Patients

Seq Age Sex Outcome Treatment
1 UNK