Lineage 26010008Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI M684260100081), received between Apr 6, 2020 and Feb 28, 2024 — classified as 7 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 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.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 28, 2024Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, LYSIS ? SOCKET/ADVERSE SOFT TISSUE REACTION TO PARTICULATE DEBRIS SIDE: R REVISION NJR: (B)(4). GENDER: F EXPLANTED: ACETABULAR CUP, MODULAR HEAD, ACETABULAR LINER

  Patient problems: Metal Related Pathology; Osteolysis

  MAUDE report 18796626 ↗
• InjuryFeb 27, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  ALLEGEDLY, DISLOCATION/SUBLUXATION/UNEXPLAINED PAIN/OTHER SIDE: R; REVISION NJR: 2184492; GENDER: F; EXPLANTED: FEMORAL STEM, ACETABULAR CUP.

  Patient problems: Pain

  MAUDE report 18793225 ↗
• InjuryDec 22, 2022Loss of Osseointegration; Malposition of Device; Naturally Worn; Loss of Osseointegration; Malposition of Device; Naturally Worn

  ALLEGEDLY, PATIENT WAS REVISED DUE TO LOOSENING - SOCKET/LYSIS-SOCKET/MALALIGNMENT-SOCKET/WEAR OF ACETABULAR COMPONENT REVISION NJR NUMBER: (B)(4). SIDE:L. PRIMARY ASA: P2 - MILD DISEASE NOT INCAPACITATING. PRODUCTS NO REVISED: PRODUCT ID: PHA05506, LOT: 89904172, QTY: 1. PRODUCT ID: PHA01204, LOT: 99926678, QTY: 1.

  Patient problems: Osteolysis

  MAUDE report 16035142 ↗
• InjuryApr 1, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  ALLEGEDLY, PATIENT WAS REVISED DUE TO DISLOCATION/SUBLUXATION COMPONENTS NOT REVISED : PRODUCT ID: PHA06262 / PROCOTYL L BEADED AND HA COATED CUP SIZE 52MM / LOT# 58567095; PRODUCT ID: PPR67604/ ANCA-FIT HA COATED ANATOMIC FEMORAL STEM SIZE 11 RIGHT / LOT# 28531335; REVISION NJR NUMBER: (B)(4); SIDE:R; PRIMARY ASA: P2 - MILD DISEASE NOT INCAPACITATING.

  Patient problems: Insufficient Information

  MAUDE report 13981306 ↗
• InjuryJan 6, 2022Appropriate Device Problem Term/Code Not Available

  SAE# (B)(4). ALLEGEDLY, THE PATIENT STARTED HAVING LT HIP PAIN 3 WEEKS AFTER SURGERY. MULTIPLE ATTEMPTS TO RELIEF THE PAIN WITH CORTICOSTEROID INJECTIONS INTRA-ARTICULAR WITH NO SUCCESS. THE PATIENT UNDERWENT A SURGICAL INTERVENTION FOR RELEASE OF THE PSOAS TENDON ON (B)(6) 2018. THE PAIN AND WEAKNESS IN THE LEFT THIGH IS STILL PERSISTENT. ADDITIONAL INFORMATION FROM CLINICAL RECEIVED ON 26/10/2021 CONFIRMING THAT COMPONENTS WERE NOT REVISED.

  Patient problems: Pain

  MAUDE report 13178641 ↗
• InjurySep 7, 2020Use of Device Problem; Device Dislodged or Dislocated; Use of Device Problem; Device Dislodged or Dislocated

  ALLEGEDLY, PATIENT WAS SQUATTING WHICH LEAD OUT A LUXATION OF THE IMPLANTED HIP; LATER IT COULD BE REPOSITIONED BY CLOSED REPOSITION.

  Patient problems: No Information

  MAUDE report 10499544 ↗
• InjuryApr 6, 2020Material Disintegration; Material Disintegration

  ALLEGEDLY, PATIENT WAS REVISED DUE TO INFECTION AND METALLOSIS IN THE NECK AND FEMORAL HEAD.

  Patient problems: Unspecified Infection

  MAUDE report 9930860 ↗