FDA Adverse Event Malfunction Summary report: N

DISTAL END CUTTER

MDR report key: 1942408 · Received December 23, 2010

Report

Report Number
2086211-2010-00124
Event Type
Malfunction
Date Received
December 23, 2010
Report Date
November 24, 2010
Manufacturer
DENTSPLY GAC
Product Code
EJB
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
DENTIST

Narratives

Additional Manufacturer Narrative · 1

WHILE NO SERIOUS INJURY RESULTED IN THIS EVENT, THERE HAS BEEN A PREVIOUS REPORT RECEIVED IN THE PAST TWO YEARS WHERE THIS MALFUNCTION RESULTED IN A SERIOUS INJURY. THEREFORE, THIS EVENT MEETS THE CRITERIA FOR REPORTABILITY PER 21 CFR 803. THE DEVICE IS AVAILABLE FOR EVAL, THOUGH HAS NOT BEEN RETURNED AS OF THIS REPORT.

Description of Event or Problem · 1

IN THIS EVENT IT WAS REPORTED THAT THE TIP OF A DISTAL END CUTTER SEPARATED; THE SEPARATED TIP WAS RETRIEVED AND NO INJURY RESULTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DISTAL END CUTTER EJB DENTSPLY GAC 09-29-5

Patients

Seq Age Sex Outcome Treatment
1 .018 X .018 BIOFORCE WIRE