FDA Adverse Event Malfunction Summary report: N

SURESMILE RETAINER

MDR report key: 19949281 · Received August 9, 2024

Report

Report Number
1649995-2024-00023
Event Type
Malfunction
Date Received
August 9, 2024
Date of Event
July 26, 2024
Report Date
October 30, 2024
Manufacturer
DENTSPLY SIRONA ORTHODONTICS INC.
Product Code
NXC
UDI-DI
00856379007269
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
DENTIST
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THERE HAS BEEN A PREVIOUS REPORT RECEIVED WHERE THIS MALFUNCTION RESULTED IN A SERIOUS INJURY. THEREFORE, IT MUST BE PRESUMED THAT RECURRENCE OF THIS MALFUNCTION COULD POSSIBLY CAUSE OR CONTRIBUTE TO A SERIOUS INJURY OR REQUIRE MEDICAL OR SURGICAL INTERVENTION TO PRECLUDE SUCH. AS SUCH, THIS EVENT IS REPORTABLE PER 21CFR PART 803. THE DEVICE IS AVAILABLE FOR EVALUATION, THOUGH HAS NOT BEEN RETURNED AS OF THIS REPORT. EVALUATION RESULTS WILL BE SUBMITTED AS THEY BECOME AVAILABLE.

Additional Manufacturer Narrative · 0

INVESTIGATION RESULTS: DHR EVALUATION: WE REVIEWED THE DHR FOR THIS (B)(6) / PATIENT ID# (B)(6) / PRACTICE ID# (B)(6), QTY. (B)(4) ITEMS ASSY-500011 (ALIGNERS), QTY. (B)(4) ITEMS ASSY-500010 (TEMPLATES), WAS PACKAGED BY THE THIRD SHIFT BY AUTO BAG AND BOX OPERATION ON APRIL 17, 2024, MANUFACTURING SUPERCELL 2, EQUIPMENT PUA-04. THE SALES ORDER WAS INSPECTED AND MET WITH THE ACCEPTANCE CRITERIA PROVIDED BY QA. FAILURE MODE - SHARP EDGES. ROOT CAUSE - NO DEFECT DURING THE MANUFACTURING PROCESS. CONCLUSION CODE - NO FAILURE FOUND.

Description of Event or Problem · 0

IN THIS EVENT IT IS REPORTED THAT SURESMILE RETAINER CAUSED CUTTING AND IRRITATION TO PATIENT'S MOUTH. ADDITIONAL INFORMATION REQUESTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2174640 SURESMILE RETAINER ALIGNER, SEQUENTIAL NXC DENTSPLY SIRONA ORTHODONTICS INC. 08566410 00856379007269

Patients

Seq Age Sex Outcome Treatment
1 15 YR Female