Lineage 26000011Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI M684260000111), received between Jan 17, 2020 and Dec 22, 2021 — classified as 3 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

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.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryDec 22, 2021Unstable; Loss of Osseointegration; Unstable; Loss of Osseointegration

  ALLEGEDLY, THE PATIENT HAS PAIN AND LOOSENING.

  Patient problems: Pain

  MAUDE report 13061353 ↗
• InjuryOct 28, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, PATIENT WAS REVISED DUE TO PAIN AND LIMB LENGTH DISCREPANCY IN HER RIGHT HIP. ALL PRODUCTS WERE REPLACED.

  Patient problems: Pain; Unequal Limb Length

  MAUDE report 10749852 ↗
• InjuryJan 17, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

  ALLEGEDLY, PATIENT SUFFERED SUBLUXATING AND PAIN. " PATIENT NEEDS MORE OFFSET" . HEAD AND LINER WERE PULLED AND OUR 15 DEGREES LINER WAS USED ALONG WITH A TJO 36MM CERAMIC +7MM HEAD.

  Patient problems: Pain

  MAUDE report 9601332 ↗