FDA Adverse Event Malfunction Summary report: N

ESTYLUS 1:5 CONTRA ANGLE ATTACHMENT

MDR report key: 2920258 · Received December 17, 2012

Report

Report Number
1419322-2012-00054
Event Type
Malfunction
Date Received
December 17, 2012
Report Date
November 20, 2012
Manufacturer
DENTSPLY PROFESSIONAL
Product Code
EKX
PMA / PMN Number
K031145
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
DENTIST

Narratives

Additional Manufacturer Narrative · 1

THOUGH NO MEDICAL/SURGICAL INTERVENTION WAS REQUIRED TO PRECLUDE A SERIOUS INJURY IN THIS EVENT, THERE HAVE BEEN PREVIOUSLY REPORTED EVENTS INCLUDING THIS DEVICE THAT RESULTED IN THE NEED FOR MEDICAL/SURGICAL INTERVENTION TO PRECLUDE PERMANENT DAMAGE TO A BODY STRUCTURE OR PERMANENT IMPAIRMENT OF A BODY FUNCTION. THEREFORE, THIS EVENT MEETS THE CRITERIA FOR REPORTABILITY PER 21 CFR PART 803. THE DEVICE IS AVAILABLE FOR EVALUATION, THOUGH RESULTS ARE NOT AVAILABLE AS OF THIS REPORT. EVALUATION RESULTS WILL BE SUBMITTED AS THEY BECOME AVAILABLE.

Description of Event or Problem · 1

IN THIS EVENT A DOCTOR REPORTED THAT AN ESTYLUS 1:5 HANDPIECE OVERHEATED; A PT WAS BURNED. HOWEVER, THEY DID NOT REQUIRE MEDICAL INTERVENTION TO TREAT THE BURN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ESTYLUS 1:5 CONTRA ANGLE ATTACHMENT EKX DENTSPLY PROFESSIONAL

Patients

Seq Age Sex Outcome Treatment
1 51 YR