Trabecular MetalRecalls & reported problems across all models

We found 24 models of Trabecular Metal by ZimVie US Corp LLC in the FDA's device registry (GUDID). Together they are named in 315 adverse event reports in the FDA's MAUDE database, received between Oct 4, 2019 and Sep 29, 2026 — classified as 290 injuries, 25 malfunctions.

The most frequently reported specific device problem is “Fracture” (66 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 Trabecular Metal problems

Trabecular Metal models

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

• Trabecular Metal™ TMTWB10

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  34 reports
• Trabecular Metal™ TMT4B10

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  30 reports
• Trabecular Metal™ TMT4B11

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  30 reports
• Trabecular Metal™ TMTB10

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  27 reports
• Trabecular Metal™ TMTB11

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  24 reports
• Trabecular Metal™ TMTWB11

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  24 reports
• Trabecular Metal™ TMT4B13

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  18 reports
• Trabecular Metal™ TMM4B10

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  17 reports
• Trabecular Metal™ TMTB13

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  17 reports
• Trabecular Metal™ TMMWB10

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  14 reports
• Trabecular Metal™ TMMB10

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  13 reports
• Trabecular Metal™ TMMWB13

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  9 reports
• Trabecular Metal™ TMT6B10

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  9 reports
• Trabecular Metal™ TMMB11

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  8 reports
• Trabecular Metal™ TMT6B11

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  8 reports
• Trabecular Metal™ TMMB13

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  7 reports
• Trabecular Metal™ TMM4B13

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  6 reports
• Trabecular Metal™ TMM4B11

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  5 reports
• Trabecular Metal™ TMM6B11

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  4 reports
• Trabecular Metal™ TMMWB11

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  3 reports
• Trabecular Metal™ TMTWB13

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  3 reports
• Trabecular Metal™ TMT6B13

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  2 reports
• Trabecular Metal™ TMTB16

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  2 reports
• Trabecular Metal™ TMM6B10

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  1 report

Recent Trabecular Metal adverse event reports

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

• MalfunctionSep 29, 2026Fracture

  It was reported implant fracture. Procedure completed with another device. Tooth site 24.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50929823 ↗
• InjuryJul 27, 2026Adverse Event Without Identified Device or Use Problem

  Patient developed Peri-implantitis at tooth site 30. X-ray taken to check implant and the implant was fractured at mesh center. Removed fractured pieces of implant and bone grafted. Inflammation pain and swelling reported as a result of the event.Patient has elected to not replace the implant at this time.

  Patient problems: Osteolysis; Swelling/ Edema; Unspecified Infection

  MAUDE report 50017174 ↗
• InjuryMay 19, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #15 LOST INTEGRATION DUE TO PERI-IMPLANTITIS AND IT WAS REMOVED. THE PATIENT WILL RETURN TO COMPLETE THE PROCEDURE.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 25218079 ↗
• InjuryMay 12, 2026Adverse Event Without Identified Device or Use Problem

  THE DOCTOR REPORTS THAT THE DENTAL IMPLANT LOCATED IN DENTAL POSITION NUMBER #17 FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS IN THE PER THAT THE PROCEDURE WAS NOT CONCLUDED BY PLACING ANOTHER IMPLANT.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 25147535 ↗
• InjuryMay 1, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT IMPLANT WAS REMOVED DUE TO BONE LOSS. PATIENT RETURNED TO CLINIC WITH SYMPTOMS OF IMPLANT SITE. RADIOGRAPHIC REVEALS BONE LOSS AROUND IMPLANT. IMPLANT REMOVED, NO IMPLANT REPLACEMENT AT THIS TIME. TOOTH NUMBER 27.

  Patient problems: Osteolysis

  MAUDE report 25057515 ↗
• InjuryFeb 17, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANTS AT TOOTH SITES #33 AND #35 WERE REMOVED DUE TO PERI-IMPLANTITIS.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 24370698 ↗
• InjuryFeb 10, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #42 WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: PAIN AND INFLAMMATION AROUND THE IMPLANT, PATIENT'S FACE WAS SWOLLEN.

  Patient problems: Inflammation; Osteolysis; Unspecified Infection

  MAUDE report 24308838 ↗
• MalfunctionFeb 6, 2026Fracture

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24283213 ↗
• MalfunctionJan 29, 2026Separation Failure

  IT WAS REPORTED THAT, DURING THE ATTEMPTED PLACEMENT OF THE IMPLANT AT TOOTH SITE #18, THE MOUNT COULD NOT DISENGAGE FROM THE IMPLANT. THE IMPLANT TORQUED TO 35NCM. A DIFFERENT IMPLANT HAD TO BE USED TO REPLACE THE IMPLANT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24210779 ↗
• MalfunctionJan 27, 2026Mechanical Problem

  IT WAS REPORTED THE IMPLANT FOR SITE 7, THE MOUNT WILL NOT DISENGAGE FROM IMPLANT. PLACED A NEW IMPLANT IN SAME PROCEDURE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24193623 ↗
• InjuryJan 27, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #13 FAILED AND WAS REMOVED DUE TO PERI-IMPLANTITIS.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 24193041 ↗
• InjuryJan 16, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANTS AT TOOTH SITES #5 AND #6 WERE REMOVED DUE TO PERI-IMPLANTITIS. THIS WAS NOTE DURING REGULAR EXAMINATIONS. THE IMPLANTS WERE REPLACED.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 24101278 ↗
• MalfunctionJan 5, 2026Detachment of Device or Device Component

  IT WAS REPORTED THAT THE FIXTURE MOUNT WAS NOT ATTACHED TO THE IMPLANT. THE PROCEDURE WAS COMPLETED WITH ANOTHER IMPLANT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23967959 ↗
• InjuryDec 17, 2025Adverse 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

  MAUDE report 23831506 ↗
• InjuryDec 16, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Osteolysis

  MAUDE report 23822249 ↗

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