LTX LTX310Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00844868009719), received between Jun 15, 2021 and May 27, 2022 — classified as 4 injuries.

The most frequently reported specific device problem is “Unintended Movement” (2 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. 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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryMay 27, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE DOCTOR REPORTS THAT DENTAL IMPLANTS LOCATED IN UNKNOWN DENTAL POSITIONS FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS THAT HE HAS PERFORMED A BONE CURETTAGE AND THAT THE PATIENT DID NOT SUFFER ANY NEGATIVE IMPACT ON HIS HEALTH AS A RESULT OF THE EVENT. THE DOCTOR REPORTED: INFLAMMATION.

  Patient problems: Inflammation; Osteolysis; Unspecified Infection

  MAUDE report 14520339 ↗
• InjurySep 2, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PERI-IMPLANTITIS WAS DENOTED ON THE IMPLANT SITE. INFLAMMATION WAS REPORTED AS A CONSEQUENCE OF THE EVENT.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 12414014 ↗
• InjuryJun 15, 2021Adverse Event Without Identified Device or Use Problem; Unintended Movement; Adverse Event Without Identified Device or Use Problem; Unintended Movement

  IT WAS REPORTED THAT THE IMPLANTS WERE REMOVED DUE TO PERI-IMPLANTITIS. MOBILITY WAS REPORTED AS A RESULT OF THE EVENT. TOOTH LOCATION IS UNKNOWN. BONE GRAFT HAS BEEN MADE.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 12001803 ↗
• InjuryJun 15, 2021Adverse Event Without Identified Device or Use Problem; Unintended Movement; Adverse Event Without Identified Device or Use Problem; Unintended Movement

  IT WAS REPORTED THAT THE IMPLANTS WERE REMOVED DUE TO PERI-IMPLANTITIS. MOBILITY WAS REPORTED AS A RESULT OF THE EVENT. TOOTH LOCATION IS UNKNOWN. BONE GRAFT HAS BEEN MADE.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 12001778 ↗