CONSERVE® 38NS0N35Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI M68438NS0N351), received between Feb 17, 2020 and May 19, 2021 — classified as 4 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 19, 2021Appropriate Device Problem Term/Code Not Available

  ALLEGEDLY, PATIENT WAS REVISED DUE TO PAIN AND INFECTION. COMPONENTS NOT REVISED: DYNASTY® BF SHELL PRIMARY 58MM GROUP G PRODUCT ID: DBFPGG58 LOT NUMBER: 1817132 PROFEMUR® PRESERVE CLASSIC SIZE 9 VARUS 8DG HIP STEM PRODUCT ID: PPRCLE09 LOT NUMBER: 1793809

  Patient problems: Pain; Unspecified Infection

  MAUDE report 11849000 ↗
• InjuryMar 18, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, FOR UNKNOWN REASONS PATIENT RECEIVED A REVISION.

  Patient problems: No Information

  MAUDE report 9847344 ↗
• InjuryFeb 20, 2020Material Disintegration; Material Disintegration

  ALLEGEDLY, PATIENT PRESENTED ELEVATED COBALT ION LEVELS AND PAIN. THE DEVICE FAILED DUE TO CORROSION AT THE NECK-STEM JUNCTION OF THE DEVICE, CORROSION ON THE OBLONG TAPER WHERE THE NECK WAS SEATED IN THE POCKET OF THE PROFEMUR TITANIUM STEM, WHICH CAUSED ADDUCTOR DAMAGE, SOFT TISSUE REACTION AND PSEUDOTUMOR REACTION. DURING THE REVISION THE SURGEON REMOVED THE FAILED COMPONENTS OF THE PROFEMUR TOTAL HIP SYSTEM.

  Patient problems: Pain; Reaction

  MAUDE report 9733128 ↗
• InjuryFeb 17, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, PATIENT WAS REVISED DUE TO ELEVATED COBALT ION LEVELS, PAIN AND STIFFENS OF THE HIP. IT WAS DISCOVERED THAT THE DEVICE FAILED DUE TO CORROSION OF THE OBLONG TAPER OF MODULAR NECK WHERE IT SEATED IN THE POCKED OF THE TITANIUM STEM.

  Patient problems: Pain

  MAUDE report 9716991 ↗