FDA Adverse Event Injury Summary report: N

CARRIERE SLX 3D

MDR report key: 17847057 · Received September 29, 2023

Report

Report Number
2081322-2023-00003
Event Type
Injury
Date Received
September 29, 2023
Date of Event
January 19, 2023
Report Date
September 29, 2023
Manufacturer
ORTHO ORGANIZERS, INC.
Product Code
EJF
UDI-DI
00190707048273
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
DENTIST
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE CARRIERE SLX 3D BRACKETS ARE STAINLESS STEEL, PASSIVE, SELF-LIGATING ORTHODONTIC BRACKETS THAT DIRECTLY BOND TO THE TEETH TO PROVIDE A TREATMENT SOLUTION FOR PATIENTS WITH MALOCCLUSIONS OF PRIMARY, PERMANENT, OR MIXED DENTITION. IT WAS REPORTED IN THE CUSTOMER COMPLAINT FORM THAT BRACKET LR4 HAD SHARP EDGES CAUSING CHEEK IRRITATION, CUTTING THE CHEEK ON THE LOWER RIGHT OF THE PATIENT AND CAUSING LARGE SORES THAT DID NOT HEAL. THE SYMPTOMS BEGAN THE DAY AFTER THE BRACKET WAS PLACED. THE BRACKET NEEDED TO BE REMOVED AND REPLACED WITH A DIFFERENT BRAND. THE 38-YEAR OLD FEMALE PATIENT WAS PRESCRIBED KENALOG IN ORABASE, A TOPICAL STEROID. SHE WAS ALSO ADVISED TO TAKE OTC PAIN MEDICATION SUCH AS IBUPROFEN AND TYLENOL. DUE TO THE FACT THAT PRESCRIPTION AND OTC MEDICATIONS WERE GIVEN, ORTHO ORGANIZERS DECIDED TO REPORT THIS COMPLAINT TO THE FDA.

Description of Event or Problem · 0

IT WAS REPORTED IN THE CUSTOMER COMPLAINT FORM THAT BRACKET LR4 HAD SHARP EDGES CAUSING CHEEK IRRITATION, CUTTING THE CHEEK ON THE LOWER RIGHT OF THE PATIENT AND CAUSING LARGE SORES THAT DID NOT HEAL. THE SYMPTOMS BEGAN THE DAY AFTER THE BRACKET WAS PLACED. THE BRACKET NEEDED TO BE REMOVED AND REPLACED WITH A DIFFERENT BRAND. THE 38-YEAR OLD FEMALE PATIENT WAS PRESCRIBED KENALOG IN ORABASE, A TOPICAL STEROID. SHE WAS ALSO ADVISED TO TAKE OTC PAIN MEDICATION SUCH AS IBUPROFEN AND TYLENOL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2271840 CARRIERE SLX 3D ORTHODONTIC METAL BRACKETS EJF ORTHO ORGANIZERS, INC. 777-LR4-HK-10 00190707048273

Patients

Seq Age Sex Outcome Treatment
1 38 YR Female Required Intervention