CONSERVE® 38015000Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI M684380150001), received between Jul 23, 2019 and Feb 28, 2024 — classified as 4 injuries.

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

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

  ALLEGEDLY, UNEXPLAINED PAIN SIDE: L REVISION NJR: (B)(4). GENDER: M EXPLANTED: FEMORAL STEM, ACETABULAR CUP

  Patient problems: Pain

  MAUDE report 18796770 ↗
• InjuryJul 13, 2021Corroded; Corroded

  ALLEGEDLY, PATIENT REVISED DUE TO LOOSENING, METAL ON METAL TOTAL HIP WITH SOME CORROSION OF THE METAL FEMORAL HEAD AND TRUNNION INTERFACE. (RIGHT HIP).

  Patient problems: Metal Related Pathology

  MAUDE report 12158882 ↗
• InjuryJul 23, 2019Material Disintegration; Material Disintegration

  ALLEGEDLY THE PATIENT IS EXPERIENCING MOM COMPLICATIONS (LEFT). THE PATIENT HAS NOT YET SCHEDULED AN EXPLANTATION OF THE HIP IMPLANT. ADDITIONAL INFORMATION RECEIVED FROM LITIGATION ON 07/13/2019. ALLEGEDLY THE PATIENT WAS REVISED DUE TO MOM COMPLICATIONS: PAIN; METALLOSIS; INFLAMMATION; PSEUDO TUMORS; AND BONE EROSION.

  Patient problems: Inflammation; Pain; Reaction

  MAUDE report 8817181 ↗
• InjuryJul 23, 2019Material Disintegration; Material Disintegration

  ALLEGEDLY THE PATIENT WAS REVISED DUE TO MOM COMPLICATIONS: PAIN; METALLOSIS; INFLAMMATION; PSEUDO TUMORS AND BONE EROSION.

  Patient problems: Inflammation; Pain; Reaction

  MAUDE report 8816231 ↗