FDA Adverse Event Malfunction Summary report: N

1/2 SIZE PERF BASKET LID 247X257MM

MDR report key: 6623182 · Received June 8, 2017

Report

Report Number
9610612-2017-00298
Event Type
Malfunction
Date Received
June 8, 2017
Date of Event
May 14, 2017
Report Date
June 8, 2017
Manufacturer
AESCULAP AG
Product Code
FSM
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

AESCULAP INC. (IMPORTER) IS SUBMITTING THIS REPORT ON BEHALF OF AESCULAP AG (MANUFACTURER). EXEMPTION NUMBER: E2014018. MANUFACTURING SITE EVALUATION: EVALUATION ON-GOING.

Description of Event or Problem · 0

COUNTRY OF COMPLAINT: UNITED KINGDOM. IT WAS REPORTED THAT THERE WERE THREE DIFFERENT INCIDENTS WITH THREE DIFFERENT PATIENTS. INCIDENT DETAILS: DURING A DENTAL SURGERY THE DRILL OVERHEATED AND IT BURNED THE INSIDE OF THE PATIENT'S MOUTH. THE DRILL STILL HAS PARTS OF THE SOFT TISSUE FROM THE PATIENT'S MOUTH. DURING A DENTAL SURGERY THE HAND PIECE STARTED SMOKING, THE HAND PIECE WAS CHANGED AND THE SURGERY WAS ABLE TO BE COMPLETED. DURING A DENTAL SURGERY THE OIL INSIDE THE DRILL STARTED LEAKING INSIDE THE PATIENT'S MOUTH. NO HARM TO THE PATIENT. ALL MED WATCH SUBMISSIONS RELATED TO THIS REPORT ARE: 9610612-2017-00296, 9610612-2017-00297, 9610612-2017-00298. COMPONENTS IN USE LISTED AS CONCOMITANT DEVICES ARE: GD450M / MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM (X3). GD678 / MICROSPEED UNI MICRO 150 MOTOR (X3). GD672 / MICROSPEED UNI MOTOR CABLE F/FOOT CTRL. (X3).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
404353 1/2 SIZE PERF BASKET LID 247X257MM WIRE BASKETS/TRAYS F.FULL/HALF SIZE FSM AESCULAP AG JF117R

Patients

Seq Age Sex Outcome Treatment
1 Other GD450MM / MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM| GD672 / MICROSPEED UNI MOTOR CABLE F/FOOT CTRL.| GD678 / MICROSPEED UNI MICRO 150 MOTOR