Lineage 26012805Recalls & reported problems
Microport Orthopedics Inc. · COCR FEMORAL HEAD 28MM SLT TAPER +10.5MM NECK · 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 M684260128051), received between Oct 1, 2019 and Aug 28, 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
- Pain2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 28, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY PATIENT POTENTIALLY HAS PAIN AS WELL AS A POSSIBLE SEROMA. DUAL MOBILITY LINER FROM STRYKER AND OUR 28MM + 10.5 HEAD WERE REPLACED WITH THE SAME PRODUCTS IN THE SAME SIZES. LEFT HIP. ADDITIONAL INFORMATION: "THIS IS THE SECOND REVISION FOR THIS PATIENT (INCIDENT GROUPS: 16010098 & 16010101).''
Patient problems: Pain
MAUDE report 10465979 ↗InjuryOct 1, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
PAIN IN THE LATERAL PROXIMAL FEMUR, STEM CAME OUT WITH THE NECK AND HEAD. STRYKER STEM AND HEAD WENT IN AND NONE OF OUR IMPLANT WENT IT.
Patient problems: Pain
MAUDE report 9142772 ↗
Other Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented devices
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- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 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.
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