FDA Adverse Event Malfunction Summary report: N

GENTLEPOWER LUX CONTRA ANGLE 25LPA

MDR report key: 2591392 · Received May 24, 2012

Report

Report Number
3003637274-2012-00030
Event Type
Malfunction
Date Received
May 24, 2012
Date of Event
March 14, 2012
Report Date
April 30, 2012
Manufacturer
KAVO DENTAL GMBH
Product Code
EFB
PMA / PMN Number
K073478
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
HI, US
Reporter Occupation
DENTIST

Narratives

Additional Manufacturer Narrative · 1

DURING A STANDARD TREATMENT, A DENTAL ELECTRICAL HANDPIECE GOT HOT AND BURNED THE PTS CHEEK TO THE DIAMETER OF THE BACK CAP. THE PT RECEIVED SOME OTC VITAMINE E OIL FOR THE BURN. NO FURTHER MEDICAL CARE WAS NECESSARY. THE ANALYSIS DID SHOW THAT THE HEAD HAD BEEN DENTED AT THE BACKCAP BUT DID NOT CAUSE THE BACK CAP BUTTON TO STICK IN. EXPERIENCE SHOWS THAT THIS IS USUALLY THE RESULT OF A STRONG HIT LIKE E.G. A DROP DURING THE REPROCESSING. ALSO THE BEARINGS HAVE BEEN GRINDING WHICH COULD BE NORMAL WEAR OR POSSIBLY STRONGER WEAR CAUSED BY THE SLIGHT DEFORMATION OF THE HEAD. DURING THE TEST RUN THE HEAT UP WAS REPRODUCIBLE. THE USER INSTRUCTION REQUIRES A VISUAL AND FUNCTIONAL INSPECTION PRIOR TO EACH TREATMENT WHICH SHOWS IF DEVICE IS RUNNING OUT OF SPECIFICATION AND IS HENCE MANDATORY. REPORTED DUE TO THE 2 YR PRESUMPTION RULE.

Description of Event or Problem · 1

DURING A STANDARD TREATMENT, A DENTAL ELECTRICAL HANDPIECE GOT HOT AND BURNED THE PTS CHEEK TO THE DIAMETER OF THE BACK CAP. THE PT RECEIVED SOME OTC VITAMINE E OIL FOR THE BURN. NO FURTHER MEDICAL CARE WAS NECESSARY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GENTLEPOWER LUX CONTRA ANGLE 25LPA DENTAL HANDPIECE EFB KAVO DENTAL GMBH 25LPA

Patients

Seq Age Sex Outcome Treatment
1 62 YR