inforMED
InjuryEMA

RELYX ULTIMATE ADHESIVE RESIN CEMENT

Received Aug 7, 2015

Report 9611385-2015-00008 · MDR key 4990597

Device

Catalog number

56890

Product problems

  • Patient-Device Incompatibility

Patient

Not reported

  • Sensitivity of Teeth

Narrative

Additional Manufacturer Narrative

3M ESPE REC'D THIS REPORT ON JULY 14, 2015 AND HAS ATTEMPTED TO OBTAIN MORE SPECIFIC INFORMATION. HOWEVER, BECAUSE THE REPORTED EVENTS HAPPENED SOMETIMES BETWEEN 2013 AND 2015 AND BECAUSE THE DENTIST WAS NOT WILLING OR ABLE TO PROVIDE ADDITIONAL INFORMATION, PATIENT-SPECIFIC REPORTING IS NOT POSSIBLE. SINCE THIS EVENT INVOLVED THREE MEDICAL DEVICES, THREE MANUFACTURER REPORTS ARE BEING SUBMITTED. THIS REPORT DESCRIBES THE SECOND DEVICE. MFR REPORT NUMBERS 3005174370-2015-00048 AND 9611385-2015-00009, DESCRIBE THE FIRST AND THIRD DEVICE, RESPECTFULLY.

Description of Event or Problem

A DENTIST REPORTED THAT 2-3 PATIENTS HAD NEED FOR ENDODONTIC TREATMENT. THESE PATIENTS HAD DENTAL RESTORATIONS MADE FROM 3M ESPE LAVA ULTIMATE CAD/CAM RESTORATIVE FOR CEREC, WHICH WERE SEATED WITH 3M ESPE RELYX ULTIMATE CEMENT AND 3M ESPE SCOTCHBOND UNIVERSAL ADHESIVE. THE REPORTING DENTIST INDICATED THAT LEAKAGE AT THE MARGIN LED TO CARIES UNDER THE CROWN. BECAUSE THE EVENTS OCCURRED DURING THE TIME PERIOD OF 2013 TO 2015, NO FURTHER PATIENT-SPECIFIC INFORMATION WAS AVAILABLE.