CONSERVE® 38HM1052Recalls & reported problems
Microport Orthopedics Inc. · CONSERVE® HM FEMORAL COMPONENT CEMENTED 52MM · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 M68438HM10521), received between Aug 19, 2020 and Aug 19, 2020 — classified as 2 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
Device problems
- Material Disintegration2
- Corroded1
Patient problems
- Pain1
- Reaction1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 19, 2020Corroded; Material Disintegration; Corroded; Material Disintegration
ALLEGEDLY, PATIENT WAS REVISED DUE TO ADVERSE TISSUE REACTION TO METAL DEBRIS, CORROSION AND RESULTANT METAL IONS.
Patient problems: Reaction
MAUDE report 10428837 ↗InjuryAug 19, 2020Material Disintegration; Material Disintegration
ALLEGEDLY, PATIENT HAS BEEN EXPERIENCING PAIN IN HIS LEFT HIP AND HIGH LEVELS OF CHROMIUM AND COBALT WERE CONFIRMED BY A BLOOD TEST. ADDITIONAL INFORMATION RECEIVED ON 07/30/2020: ADDING SCHEDULED REVISION SURGERY DATE AND PATIENT NAME.
Patient problems: Pain
MAUDE report 10428832 ↗
Other Prosthesis, Hip, Femoral, Resurfacing devices
- SYNOVO HIP COMPONENTS 01-03-0044Synovo Production · Prosthesis, Hip, Femoral, Resurfacing1 recall0 reports
- Recap Hip System US157340Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- Recap Hip System US157344Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- SYNOVO HIP COMPONENTS 01-03-0047Synovo Production · Prosthesis, Hip, Femoral, Resurfacing1 recall0 reports
- Recap Hip System US157342Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- 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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page