Eztetic CT318Recalls & reported problems

Summary

The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00889024343917), received between Feb 23, 2021 and May 12, 2026 — classified as 15 injuries.

The most frequently reported specific device problem is “Fracture” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.

• InjuryMay 12, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT AN IMPLANT AT TOOTH SITE # 14 WAS REMOVED DUE TO A PERI-IMPLANTITIS. PAIN WAS REPORTED AS A RESULT OF THE EVENT.

  Patient problems: Osteolysis; Pain; Unspecified Infection

  MAUDE report 25147179 ↗
• InjuryMar 26, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT COMPLAINED OF DISCOMFORT AROUND THE IMPLANT AT TOOTH SITE #19. THE DOCTOR CHECKED AND STATED THAT THE IMPLANT DID NOT INTEGRATE DUE TO BONE LOSS. THE IMPLANT WAS REMOVED. SYMPTOMS AS A RESULT OF THE EVENT: PAIN AND DISCOMFORT.

  Patient problems: Discomfort; Osteolysis; Pain

  MAUDE report 24697602 ↗
• InjuryMar 24, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT CAME IN WITH DISCOMFORT AROUND THE IMPLANT AT TOOTH SITE #20. THE DOCTOR CHECKED AND THE PATIENT HAS PERI-IMPLANTITIS WITH ABSCESS. THE IMPLANT WAS REMOVED. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS AND INFLAMMATION.

  Patient problems: Abscess; Inflammation; Osteolysis

  MAUDE report 24674517 ↗
• InjuryMay 8, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO ADDITIONAL EVENT INFORMATION RECEIVED AT THE TIME OF THIS REPORT.

  Patient problems: Fluid Discharge; Unspecified Infection

  MAUDE report 19270915 ↗
• InjuryMar 5, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO ADDITIONAL EVENT INFORMATION RECEIVED AT THE TIME OF THIS REPORT.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 18839306 ↗
• InjuryOct 26, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #7 WAS REMOVED DUE TO PERIIMPLANTITIS. LOOSE PAINFUL IMPLANT PER INDICATED: SYMPTOMS AS A RESULT OF THE EVENT: INFECTION, PAIN & INFLAMMATION.

  Patient problems: Pain; Unspecified Infection

  MAUDE report 18014811 ↗
• InjuryOct 19, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT PRESENT FOR FOLLOW UP ON FAILED IMPLANT. THE PATIENT EXPERIENCED ++ BUCCAL BONE LOSS AT IMPLANT TOOTH SITE #12, WITH ASSOCIATED ABSCESS, PAIN AND SWELLING. THEREFORE, THE IMPLANT WAS REMOVED.

  Patient problems: Inflammation; Osteolysis; Pain

  MAUDE report 17963652 ↗
• InjuryOct 28, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT WAS REMOVED DUE TO AN INFECTION.

  Patient problems: Inflammation; Pain; Unspecified Infection

  MAUDE report 15690920 ↗
• InjuryOct 13, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE COVER SCREW GOT LOCKED ON THE IMPLANT AND COULDN'T BE REMOVED, WHICH RESULTED IN THE IMPLANT BEING REMOVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15596526 ↗
• InjuryJul 27, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT WAS REMOVED DUE TO INFECTION AT THE IMPLANT SITE.

  Patient problems: Inflammation; Unspecified Infection

  MAUDE report 15117822 ↗
• InjuryFeb 23, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT WAS REMOVED DUE TO INFECTION, INFLAMMATION, PAIN, REDNESS AND TENDERNESS AT THE SITE. THE PATIENT WILL NOT RETURN FOR ADDITIONAL APPOINTMENTS. TOOTH #24.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Discomfort; Inflammation; Pain; Unspecified Infection

  MAUDE report 13584515 ↗
• InjuryJan 6, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT WAS REMOVED DUE TO PERI-IMPLANTITIS. PATIENT HAD IMPLANTS PLACED (B)(6) 2021. WAITED 4-5 MONTHS FOR INTEGRATION. IMPLANT WAS STABLE + FABRICATED IMPLANT OVER DENTURE FOR MANDIBULAR. PLACEMENT OF OVER DENTURE (B)(6) 2021. IMPLANT FELL OUT (B)(6) 2021 (APPROX. DATE PER PT). CUSTOMER USED ANOTHER DEVICE TO COMPLETE THE PROCEDURE. INFLAMMATION WAS REPORTED. PATIENT WILL RETURN FOR AN ADDITIONAL APPOINTMENT: AFTER PLACEMENT WAITED 4 MONTHS OVER DENTURE. TOOTH # 27.

  Patient problems: Inflammation; Osteolysis; Unspecified Infection

  MAUDE report 13176743 ↗
• InjuryJan 6, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT WAS REMOVED DUE TO PERI-IMPLANTITIS. PATIENT HAD IMPLANT PLACED (B)(6) 2021. WAITED 4-5 MONTHS FOR INTEGRATION. IMPLANT WAS STABLE + FABRICATED IMPLANT OVER DENTURE FOR MANDIBULAR. PLACEMENT OF OVER DENTURE (B)(6) 2021. IMPLANT FELL OUT (B)(6) 2021 (APPROX. DATE PER PT). CUSTOMER USED ANOTHER DEVICE TO COMPLETE THE PROCEDURE. INFLAMMATION WAS REPORTED. PATIENT WILL RETURN FOR AN ADDITIONAL APPOINTMENT: AFTER PLACEMENT WAITED 4 MONTHS OVER DENTURE. TOOTH # 22.

  Patient problems: Inflammation; Osteolysis; Unspecified Infection

  MAUDE report 13176742 ↗
• InjuryNov 11, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DOCTOR REPORTED THE IMPLANT IN TOOTH LOCATION # 42 WAS REMOVED DUE TO PERI-IMPLANTITIS. THE IMPLANT HAD AN OVERDENTURE WHICH WAS REMOVED DUE TO THE INFECTION.

  Patient problems: Implant Pain; Inflammation; Osteolysis; Unspecified Infection

  MAUDE report 12793321 ↗
• InjuryFeb 23, 2021Fracture; Fracture

  IT WAS REPORTED THAT IMPLANT FRACTURED AT TOOTH LOCATION # 13. IMPLANT AVULSED. WILL REPLACE. AS A RESULT OF THIS EVENT, NO INJURY TO THE PATIENT REPORTED. SYMPTOMS AS A RESULT OF THE EVENT: NONE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11364629 ↗