CONSERVE® 38PF1048Recalls & reported problems
Microport Orthopedics Inc. · CONSERVE® CEMENTLESS FEMORAL COMPONENT 48MM · Class 2 · Implant
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M68438PF10481), received between Feb 3, 2020 and Jul 24, 2020 — classified as 2 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information2
Patient problems
- Bone Fracture(s)1
- Unspecified Infection1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 24, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, XRAY SHOWED A FRACTURED AT THE FEMORAL NECK OF HIS RIGHT SIDE , JUST BELOW THE LEVEL OF PROSTHESIS. A VISIT WITH DR (B)(6) ON (B)(6) 2019 INDICATED THE STRESS FRACTURED WAS HEALED , AND SUBJECT WAS GRADUALLY RETURNING TO REGULAR ACTIVITIES. SUBJECT WAS TREATED NON-OPERATIVELY AND RECEIVED TYLENOL AND TRAMADOL WHILE IN THE EMERGENCY DEPARTMENT.
Patient problems: Bone Fracture(s)
MAUDE report 10320084 ↗InjuryFeb 3, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED DUE TO DEEP WOUND INFECTION. ADDITIONAL INFORMATION : LEFT SIDE.
Patient problems: Unspecified Infection
MAUDE report 9659562 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.