CONSERVE® 38PF1052Recalls & reported problems
Microport Orthopedics Inc. · CONSERVE® CEMENTLESS FEMORAL COMPONENT 52MM · Class 2 · Implant
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI M68438PF10521), received between Dec 20, 2016 and May 18, 2022 — classified as 4 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
Device problems
- Insufficient Device Problem Information3
- Fracture1
Patient problems
- Bone Fracture(s)1
- Insufficient Information1
- Metal Related Pathology1
- Pain1
- Reaction1
- Thrombosis1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryMay 18, 2022Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, A POTENTIAL COMPLAINT HAS BEEN RECEIVED BY MICROPORT ORTHOPEDICS LEGAL DEPARTMENT. MEDICAL RECORDS RELATED TO PRIMARY SURGERY MENTION THAT X-RAYS DEMONSTRATED RIGHT HIP DEGENERATIVE ARTHRITIS. THERE MAY BE A POSSIBLE FAILURE, WHICH IS UNKNOWN AS NO ADDITIONAL INFORMATION HAS BEEN RECEIVED.
Patient problems: Insufficient Information
MAUDE report 14427658 ↗InjuryApr 28, 2021Fracture
SAE # (B)(4). ALLEGEDLY, THE PATIENT HAD A SMALL STUMBLE. IMAGING SHOWED A RIGHT NECK OF FEMUR FRACTURE. ALL COMPONENTS WERE REVISED.
Patient problems: Bone Fracture(s)
MAUDE report 11739633 ↗InjuryDec 5, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
(B)(6): ALLEGEDLY , PATIENT WAS DIAGNOSED WITH DEEP VEIN THROMBOSIS.
Patient problems: Thrombosis
MAUDE report 9418476 ↗InjuryDec 20, 2016Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT REVISED DUE TO METALLOSIS. RIGHT (B)(6).
Patient problems: Metal Related Pathology; Pain; Reaction
MAUDE report 6191243 ↗
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- Recap Hip System US157346Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- SYNOVO HIP COMPONENTS 01-03-0045Synovo Production · Prosthesis, Hip, Femoral, Resurfacing1 recall0 reports
- Recap Hip System US157356Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.