CONSERVE® 38031050Recalls & reported problems
Microport Orthopedics Inc. · CONSERVE® FEMORAL RESURFACING HEAD 50MM · Class 2 · Implant
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI M684380310501), received between Jul 23, 2019 and Aug 12, 2021 — classified as 3 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
- Adverse Event Without Identified Device or Use Problem1
- No Apparent Adverse Event1
Patient problems
- Metal Related Pathology2
- Reaction1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryAug 12, 2021Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event; Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event
ALLEGEDLY, PATIENT WAS REVISED DUE TO OTHER/ ADVERSE SOFT TISSUE REACTION TO PARTICULATE DEBRIS. REVISION NJR NUMBER: (B)(4). SIDE: L. PRIMARY ASA: P2: MILD DISEASE NOT INCAPACITATING.
Patient problems: Metal Related Pathology
MAUDE report 12315297 ↗InjuryNov 3, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED DUE TO ADVERSE SOFT TISSUE REACTION TO PARTICLE DEBRIS REVISION NJR NUMBER: (B)(4). SIDE: L. PRIMARY ASA: P1 - FIT AND HEALTHY. (B)(4).
Patient problems: Metal Related Pathology
MAUDE report 10777527 ↗InjuryJul 23, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY THE PATIENT WAS REVISED DUE TO ADVERSE TISSUE REACTION TO PARTICLE DEBRIS REVISION (B)(6); SIDE: R; PRIMARY ASA: P2-MILD DISEASE NOT INCAPACITATING. THE FOLLOWING COMPONENT HAS NO ALLEGED DEFICIENCY AND WAS NOT REVISED DURING THIS SURGERY: CONSERVE® THIN SHELL HA COATED 50MM ID 56MM OD BEADED 38HA5056 LOT # 027388279 QTY. 1.
Patient problems: Reaction
MAUDE report 8815625 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.