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XiVE® 32252443Recalls & reported problems

Dentsply Implants Manufacturing GmbH · XiVE® TG plus Implant D3.8/L13 · Class 2 · Implant

Quick summary

This XiVE TG plus dental implant is placed in the jaw to replace a tooth root. The 26 reports mainly describe the implant failing to bond with bone and being lost, sometimes with infection or inflammation. There were 26 reports, no deaths, and 26 injuries. No recalls name this device; reports fell from 12 in the previous 12 months to 0 in the most recent 12 months.

AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.

Adverse event reports
26
Deaths reported
0
Injuries reported
26
Recalls naming it
0

Summary

The FDA's MAUDE database contains 26 adverse event reports that list this exact device (DI 07392532212192), received between Aug 15, 2023 and Jul 11, 2025 — classified as 26 injuries.

The most frequently reported specific device problem is “Loss of Osseointegration” (15 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, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 1 reportsJan 2024: 2 reportsFeb 2024: 0 reportsMar 2024: 3 reportsApr 2024: 1 reportsMay 2024: 1 reportsJun 2024: 1 reportsJul 2024: 1 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 1 reportsJan 2025: 1 reportsFeb 2025: 2 reportsMar 2025: 3 reportsApr 2025: 0 reportsMay 2025: 4 reportsJun 2025: 0 reportsJul 2025: 1 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520264
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Loss of Osseointegration15
  • Failure to Osseointegrate11

Patient problems

  • Failure of Implant26
  • Pocket Erosion6
  • Unspecified Infection6
  • Inflammation3
  • Osteolysis2

Recent adverse event reports

The 25 most recent of 26 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 11, 2025Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22487098 ↗
  • InjuryMay 24, 2025Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22081964 ↗
  • InjuryMay 15, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Inflammation

    MAUDE report 22027161 ↗
  • InjuryMay 13, 2025Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22012721 ↗
  • InjuryMay 13, 2025Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22012615 ↗
  • InjuryMar 26, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Unspecified Infection

    MAUDE report 21700392 ↗
  • InjuryMar 26, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Unspecified Infection

    MAUDE report 21700330 ↗
  • InjuryMar 26, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Unspecified Infection

    MAUDE report 21700205 ↗
  • InjuryFeb 21, 2025Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Inflammation; Pocket Erosion

    MAUDE report 21432325 ↗
  • InjuryFeb 13, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21373262 ↗
  • InjuryJan 23, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21217554 ↗
  • InjuryDec 10, 2024Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 20895856 ↗
  • InjuryJul 2, 2024Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 19654188 ↗
  • InjuryJun 24, 2024Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 19593485 ↗
  • InjuryMay 7, 2024Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Pocket Erosion

    MAUDE report 19258545 ↗
  • InjuryApr 10, 2024Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 19078176 ↗
  • InjuryMar 13, 2024Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Inflammation; Pocket Erosion

    MAUDE report 18894279 ↗
  • InjuryMar 5, 2024Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Pocket Erosion

    MAUDE report 18836291 ↗
  • InjuryMar 5, 2024Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Pocket Erosion

    MAUDE report 18835680 ↗
  • InjuryJan 16, 2024Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Pocket Erosion

    MAUDE report 18516749 ↗
  • InjuryJan 10, 2024Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 18483287 ↗
  • InjuryDec 19, 2023Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Osteolysis

    MAUDE report 18354140 ↗
  • InjurySep 27, 2023Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Unspecified Infection

    MAUDE report 17825501 ↗
  • InjurySep 27, 2023Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Unspecified Infection

    MAUDE report 17824826 ↗
  • InjurySep 27, 2023Loss of Osseointegration; Loss of Osseointegration

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant; Unspecified Infection

    MAUDE report 17824519 ↗

Other IMPLANT, ENDOSSEOUS, ROOT-FORM devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.