Lineage 72003252Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M684720032521), received between Mar 10, 2020 and Jun 24, 2022 — classified as 2 injuries.

The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 24, 2022Break; Break

  ALLEGEDLY, BROKEN CERAMIC LINER, THE CUP REVISED AND NEW BIOLOX HEAD WITH SLEEVE IMPLANTED. THE CUP WAS DAMAGED IN THE REMOVAL PROCESS. COMPONENTS NOT REVISED: PRODUCT: PROFEMUR® NECK NEUTRAL LONG PRODUCT ID: PHA01204, LOT#: 038561200 QTY:1. PRODUCT: PROFEMUR® TL STEM SZ 3 PRODUCT ID: PRTL0023, LOT#: 027395031, QTY:1.

  Patient problems: Insufficient Information

  MAUDE report 14800294 ↗
• InjuryMar 10, 2020Break; Noise, Audible; Break; Noise, Audible

  ALLEGEDLY, SUBJECT WAS SEEN IN EMERGENCY ROOM WITH RIGHT HIP PAIN FOR 2 WEEKS, CRUNCHING WITH MOTION AND DIFFICULTY AMBULATING. LINER FRACTURE WAS CONFIRMED BY X RAY AND CT OF THE HIP. SUBJECT HAD A REVISION AND REMOVAL OF THE ORIGINAL ACETABULAR, LINER, MODULAR NECK AND FEMORAL HEAD AND WAS DISCHARGED ON (B)(6) 2015.

  Patient problems: Loss of Range of Motion; Pain

  MAUDE report 9813945 ↗