EzteticRecalls & reported problems across all models

We found 15 models of Eztetic by ZimVie US Corp LLC in the FDA's device registry (GUDID). Together they are named in 382 adverse event reports in the FDA's MAUDE database, received between Apr 24, 2019 and Sep 29, 2026 — classified as 361 injuries, 21 malfunctions.

The most frequently reported specific device problem is “Fracture” (18 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported Eztetic problems

Eztetic models

15 models, most reported first. Each model has its own page with its reports, recalls and device details.

• Eztetic™ CT3111

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  70 reports
• Eztetic™ CM3111

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  65 reports
• Eztetic™ CT3110

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  64 reports
• Eztetic™ CM3110

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  60 reports
• Eztetic™ CT3113

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  42 reports
• Eztetic™ CM3113

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  38 reports
• Eztetic CT318

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  15 reports
• Eztetic™ CM318

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  11 reports
• Eztetic™ CM3116

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  7 reports
• Eztetic™ CANP31S

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  3 reports
• Eztetic™ CANP31A

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  2 reports
• Eztetic™ CT3116

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  2 reports
• Eztetic™ CHCNP43

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  1 report
• Eztetic® CITNP33

  ACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS
  1 report
• Eztetic™ CTANP31

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  1 report

Recent Eztetic adverse event reports

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

• InjurySep 29, 2026Separation Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50929465 ↗
• InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem

  It was reported that an implant was removed due to a peri-implantitis at tooth site 33.Pain was reported as a consequence.

  Patient problems: Osteolysis; Pain; Unspecified Infection

  MAUDE report 50914381 ↗
• InjurySep 17, 2026Adverse Event Without Identified Device or Use Problem

  It was reported that an implant was removed due to a bone loss. The patient noted a small bump on the gingiva near the implant placed in site #23. Radiographs revealed some bone loss. A flap was raised revealing #23 implant had significant buccal bone recession exposing several implant threads.Abscess, pain and inflammation were reported as a consequence.

  Patient problems: Abscess; Osteolysis; Pain

  MAUDE report 50798606 ↗
• InjurySep 14, 2026Adverse Event Without Identified Device or Use Problem

  It was reported that an implant was removed due to an infection at tooth site 28. Patient suffered from inflammation and tenderness.Bone density type: II.

  Patient problems: Inflammation; Unspecified Infection

  MAUDE report 50750877 ↗
• InjuryJun 10, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE FIXTURE (IMPLANT) AT TOOTH SITE #7 WAS MOBILE AND WAS REMOVED DUE INFECTION AND BONE LOSS. THE SITE WAS CLEANED AND BONE GRAFTING AND COLLAGEN MEMBRANE WERE USED. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS.

  Patient problems: Abscess; Osteolysis; Unspecified Infection

  MAUDE report 25461692 ↗
• InjuryJun 5, 2026Fracture

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #24 FRACTURED AND IT HAD TO BE REMOVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25415007 ↗
• InjuryJun 2, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #23 GOT INFECTED WITH PUS DRAINAGE. THE IMPLANT ALSO LOST INTEGRATION AND WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS, INFLAMMATION, PAIN AND SWELLING.

  Patient problems: Osteolysis; Purulent Discharge; Unspecified Infection

  MAUDE report 25359277 ↗
• InjuryMay 26, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE (B)(6) WAS REMOVED DUE TO PERI-IMPLANTITIS.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 25279192 ↗
• 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 ↗
• InjuryMay 4, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT IMPLANT WAS REMOVED DUE TO BONE LOSS. LOOSE IMPLANT. TOOTH NUMBER 13.

  Patient problems: Osteolysis

  MAUDE report 25072881 ↗
• InjuryApr 28, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #24 WAS REMOVED DUE TO INFECTION AROUND THE IMPLANT AFTER PLACEMENT. AN ADDITIONAL APPOINTMENT WAS REQUIRED.

  Patient problems: Unspecified Infection

  MAUDE report 25018937 ↗
• InjuryApr 23, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #11 WAS REMOVED DUE TO INFECTION. PA WAS TAKEN. BONE WAS PLACED. AN ADDITIONAL APPOINTMENT WAS REQUIRED IN APPROXIMATELY FIVE MONTH FOR AN IMPLANT REPLACEMENT.

  Patient problems: Unspecified Infection

  MAUDE report 24972013 ↗
• InjuryApr 9, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #22 WAS REMOVED DUE TO PERI-IMPLANTITIS. DURING THE SECOND STAGE, A VESTIBULAR FISTULA WAS PRESENT, AND THE IMPLANT, SURROUNDED BY GRANULATION TISSUE WAS NOT INTEGRATED. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS.

  Patient problems: Abscess; Osteolysis; Unspecified Infection

  MAUDE report 24833272 ↗
• InjuryMar 26, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT PRESENTED FOR A SECOND STAGE PROCEDURE. A PERIODONTAL ABSCESS WAS PRESENT AT TOOTH SITE #26. THE FLAP WAS RAISED AND SEVERE BONE LOSS TO APICAL WAS NOTED ON A THIRD OF THE IMPLANT. IT WAS REVERSE TORQUED BY HAND AND THE IMPLANT WAS REMOVED.

  Patient problems: Abscess; Osteolysis; Unspecified Infection

  MAUDE report 24706383 ↗
• 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 ↗

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