FDA Adverse Event Injury Summary report: N

HERCULITE ULTRA

MDR report key: 3624756 · Received February 12, 2014

Report

Report Number
2024312-2014-00105
Event Type
Injury
Date Received
February 12, 2014
Report Date
February 3, 2014
Manufacturer
KERR CORPORATION
Product Code
EBF
PMA / PMN Number
K082671
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
DENTIST

Narratives

Additional Manufacturer Narrative · 1

THE LOT NUMBERS INVOLVED IN THE ALLEGED INCIDENTS WERE NOT RETURNED; THEREFORE, A PHYSICAL EVALUATION WAS PERFORMED ON A RETAINED SAMPLE FOR EACH OF THE LOTS, YIELDING RESULTS WITHIN SPECIFICATIONS. IN ADDITION, NO SIMILAR COMPLAINTS WERE RECEIVED WITH REGARD TO ANY OF THESE LOTS.

Additional Manufacturer Narrative · 1

ALTHOUGH THE DOCTOR IDENTIFIED FOURTEEN (14) DIFFERENT LOTS ASSOCIATED WITH NOT CURING, THE DOCTOR COULD NOT VERIFY WHICH LOT WAS USED ON THE PATIENT. THE LOTS INVOLVED IN THE ALLEGED INCIDENT INCLUDE 4586772, 4594223, 4862345, 4916637, 4982755, 4996028, 4950206, 4960403, 4201571, 4568733, 4211007, 4397297, 3694407, AND 4665691. PATIENT SPECIFICS WITH REGARD TO GENDER, AGE, AND WEIGHT WERE NOT PROVIDED. THE CURED AND UNCURED COMPOSITE WAS DRILLED OUT AND REPLACED USING A NEW HERCULITE ULTRA TIP DURING THE SAME OFFICE VISIT. TO DATE, THE PATIENT IS DOING FINE. THE PRODUCT INVOLVED IN THE ALLEGED INCIDENT HAS NOT BEEN RETURNED. AN EVALUATION OF RETAINED SAMPLES IS ANTICIPATED, BUT HAS NOT YET BEGUN.

Description of Event or Problem · 1

A DOCTOR'S OFFICE ALLEGED THAT THE HERCULITE ULTRA COMPOSITE DID NOT POLYMERIZE DURING PROCEDURES ON APPROXIMATELY TWENTY (20) PATIENTS. THIS IS THE NINETEENTH OF TWENTY (20) REPORTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
92345 HERCULITE ULTRA MATERIAL, TOOTH SHADE, RESIN EBF KERR CORPORATION

Patients

Seq Age Sex Outcome Treatment
1 Other XT BOND| FLOW-IT