FDA Adverse Event Injury Summary report: N

SMILE DIRECT CLUB CLEAR ALIGNERS ALIGN TECHNOLOGY, INC.

MDR report key: 9384059 · Received November 26, 2019

Report

Report Number
MW5091334
Event Type
Injury
Date Received
November 26, 2019
Date of Event
November 25, 2019
Report Date
November 25, 2019
Manufacturer
SMILE DIRECT CLUB / ALIGN TECHNOLOGY, INC.
Product Code
NXC
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
MA, US
Reporter Occupation
DENTIST

Narratives

Description of Event or Problem · 1

DEVICE: SMILE DIRECT CLUB ORTHODONTIC CLEAR ALIGNER; EVENT: SUSPECT THAT ALIGNERS HAVE CAUSED PT'S DENTITION TO DEVIATE FROM NORMAL OCCLUSION (ESPECIALLY ANTERIOR). PT REPORTS COMPLAINING TO THE MFR REGARDING THIS ISSUE PRIOR TO THE DATE. REPORTS A FEELING OF "PRESSURE" IN THE UL QUADRANT WHERE PT HAS MISSING TEETH #12, 13 EXAM SHOWS NO OTHER ISSUES (NO CARIES, NO BONE LOSS ETC.), HOWEVER PT IS DUE FOR A DEEP SCALING AND ROOT PLANING. PROBLEM: PT NOT EDUCATED BY MFR REGARDING POTENTIAL SIDE EFFECTS OF DEVICE. PT ADVISED THAT SOME PRESSURE FROM THE ALIGNERS IS NORMAL AS THIS IS SIGNIFYING TOOTH MOVEMENT, BUT TOO MUCH PRESSURE IS A CAUSE FOR CANCER. PT STATES THAT SHE WAS NOT GIVEN ANY INFO REGARDING THIS SIDE EFFECT, AND IS CONCERNED ABOUT THE MOVEMENT BEING TOO MUCH (POINTING TO ANTERIOR TEETH AS PRIOR) PRODUCT USE: UNCERTAIN THAT PT IS USING PRODUCT AS DIRECTED AS THERE IS NO DIRECT PROVIDER RESPONSIBLE FOR PT FU. UNCERTAIN THAT PRODUCT IS BEING MANUFACTURED AS DIRECTED AS THERE IS NO DIRECT PROVIDER RESPONSIBLE FOR IDENTIFYING IF THE PRODUCT IS MADE CORRECTLY FOR EACH ALIGNER. OUTCOME: TOOTH MOVEMENT THAT IS NOT EXPECTED OR WANTED BY THE PT. MAJORLY THE ISSUE IS THAT THE ANTERIOR TOOTH MOVEMENT DOES NOT APPEAR TO BE DESIRABLE BY THE PT, AND IS ALSO CAUSING ISSUES DUE TO ANTERIOR GUIDANCE / EXCURSIVE MOVEMENT INTERFERENCE BY THE ANTERIOR DENTITION (8/9 AND 23-26). FOR EXAMPLE: PT POINTS TO #9 BEING KICKED OUT BY A MILLIMETER, AND THE 23-26 LOWER ANTERIORS ARE INSICALLY POSITIONED COMPARED TO WHERE THEY SHOULD BE (SUPRA-ERUPTED) BY ABOUT 2-3 MM. THIS IS A RECENT DEVELOPMENT FROM THE USE OF SAID PRODUCT PER PT. REQUIRED INTERVENTION: STRONGLY SUGGESTED THAT THE PT SEEK PROFESSIONAL ORTHODONTIC GUIDANCE AS CONTINUED USE OF ALIGNERS WITHOUT ANYONE THERE TO MONITOR PROGRESSION MAY NOT LEAD TO A DESIRABLE ESTHETIC RESULT AND MAY RESULT IN MAJOR ISSUES WITH PT'S OCCLUSION LONG TERM AS WELL. FDA SAFETY REPORT ID# (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1174704 SMILE DIRECT CLUB CLEAR ALIGNERS ALIGN TECHNOLOGY, INC. ALIGNER, SEQUENTIAL NXC SMILE DIRECT CLUB / ALIGN TECHNOLOGY, INC. UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 46 YR Other| R