Trabecular Metal™ TMMWB10Recalls & reported problems

Summary

The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 00889024018907), received between Mar 2, 2020 and Jan 16, 2026 — classified as 14 injuries.

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 18, 2026.

Most reported problems

Recent adverse event reports

The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.

• 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 ↗
• InjuryJun 21, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE DENTAL IMPLANT LOCATED IN DENTAL POSITION NUMBER #36 FAILED DUE TO PERI-IMPLANTITIS.

  Patient problems: Osteolysis; Pain; Unspecified Infection

  MAUDE report 22303533 ↗
• InjuryJul 26, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT RETURNED 3 WEEKS AFTER IMPLANT PLACEMENT WITH SWELLING IN THE FACE. EXAM REFLECTED PUS DRAINAGE AROUND IMPLANT AT TOOTH SITE # UNKNOWN. SYMPTOMS AS A RESULT OF THE EVENT: DRAINAGE. INFLAMMATION.

  Patient problems: Inflammation; Unspecified Infection

  MAUDE report 19843270 ↗
• InjuryMay 31, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH 14 WERE REMOVED DUE TO PERI-IMPLANTITIS. EDEMA AND INFLAMMATION WERE REPORTED AS A RESULT OF THE EVENT.

  Patient problems: Inflammation; Osteolysis; Swelling/ Edema; Unspecified Infection

  MAUDE report 17030724 ↗
• InjuryNov 29, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED INFECTION AT TOOTH 19. IMPLANT WAS REMOVED. SYMPTOMS AS A RESULT OF THE EVENT: NONE INDICATED.

  Patient problems: Unspecified Infection

  MAUDE report 15882608 ↗
• InjuryJul 28, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT ON TOOTH SITE #30 WAS REMOVED DUE TO INFECTION. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS, EDEMA.

  Patient problems: Abscess; Swelling/ Edema; Unspecified Infection

  MAUDE report 15124684 ↗
• InjuryMay 27, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT'S CBCT SCAN INDICATED UNUSUAL PATTERN OF TRABECULAR BONE, DUE TO CHRONIC SINUSITIS ACCORDING TO RADIOLOGIST. THE IMPLANT WAS REMOVED DUE TO AN INFECTION. TOOTH #3.

  Patient problems: Unspecified Infection

  MAUDE report 14526075 ↗
• InjuryApr 1, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE # 30 LOST INTEGRATION DUE TO PERI-IMPLANTITIS AT THE IMPLANT SITE AND WAS REMOVED. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS AND PAIN. THE SITE WAS GRAFTED WITH ALLOGRAFT PRIOR TO ORIGINAL IMPLANT PLACEMENT.

  Patient problems: Abscess; Osteolysis; Pain; Unspecified Infection

  MAUDE report 13978404 ↗
• InjuryMar 31, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE # 18 WAS REMOVED DUE TO BONE LOSS. SYMPTOMS AS A RESULT OF THE EVENT: PAIN.

  Patient problems: Osteolysis; Pain

  MAUDE report 13965194 ↗
• InjuryNov 13, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DOCTOR REPORTED THE IMPLANT IN TOOTH LOCATION 19 HAD LACK OF PRIMARY STABILITY AND WAS REMOVED. DOCTOR TRIED TO PLACE THE IMPLANT BUT THE BONE WAS TOO SOFT. DOCTOR DID NOT PLACE ANOTHER IMPLANT IN THE SAME PROCEDURE AND PLACED OTHER LATER ON. NOW PATIENT HAVE IMPLANT AND CONTINUE THE WILL CONTINUE THE PROCESS.

  Patient problems: No Information

  MAUDE report 10835652 ↗
• InjuryNov 6, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT IMPLANT WAS REMOVED DUE TO BONE LOSS. PATIENT COMPLAINT OF BAD TASTE ON SEVERAL OCCASIONS; HOWEVER NO SIGNS OF INFECTION WAS NOTED. DEEP POCKETING AND BONE LOSS WAS REPORTED AND IMPLANT WAS REMOVED.

  Patient problems: No Code Available

  MAUDE report 10805844 ↗
• InjuryOct 15, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DOCTOR REPORTS THAT THE TMMWB10 IMPLANT WAS PLACED (B)(6) 2020. ON (B)(6) 2020 PATIENT PRESENTED IN OFFICE AND THE IMPLANT HAD TO BE REMOVED DUE TO INFECTION. TOOTH SITE # 16. INFLAMMATION IS ALSO REPORTED.

  Patient problems: Inflammation; Unspecified Infection

  MAUDE report 10684371 ↗
• InjurySep 2, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE # UNKNOWN, FAILED DUE TO AN INFECTION AND WAS REMOVED. IMPLANT FAILED AFTER 2 WEEKS FROM THE PLACEMENT DATE, NO INJURY TO PATIENT OTHER THAN IMPLANT BEING REMOVED. NO PERMANENT IMPAIRMENT. ADDITIONAL APPOINTMENT REQUIRED: NOT INDICATED. SYMPTOMS AS A RESULT OF THE EVENT: INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 10483519 ↗
• InjuryMar 2, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT COULD NOT BE PLACED. CUSTOMER STATED THAT THE BONE WAS NOT DENSE AT THE TIME. IMPLANT WAS REMOVED AND NO OTHER IMPLANT WAS ABLE TO BE PLACED. TOOTH LOCATION 19.

  Patient problems: No Information

  MAUDE report 9776023 ↗