Lineage 26010010Recalls & reported problems
Microport Orthopedics Inc. · COCR FEMORAL HEAD 32MM SLT TAPER X-LONG NECK · Class 2 · Implant
All models of Lineage (35)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 M684260100101), received between Nov 21, 2019 and Mar 23, 2026 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information2
- Material Disintegration1
Patient problems
- No Information1
- Reaction1
- Unspecified Infection1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryMar 23, 2026Insufficient Device Problem Information
ALLEGEDLY, INFECTION WITH THE SERRATIA MARCESCENS BACTERIA. HOSPITAL SUSPECTS THAT THE ICE AND/OR THE BAGS CONTAINING IT, USED TO PREVENT POST-OPERATIVE SWALLOWING, MAY HAVE BEEN CONTAMINATED. HOSPITAL RAN TESTS ON A THIRD PATIENT THAT USED MPO PRODUCTS. THAT THIRD PATIENT'S EXAM WAS NEGATIVE, SO THEY DISCARDED MPO PRODUCTS FROM BEING THE CAUSE OF THE INFECTION. PREVIOUSLY HOSPITALIZED AT HOSPITAL (B)(6) ((B)(6) 2025).
Patient problems: Unspecified Infection
MAUDE report 24664849 ↗InjuryOct 9, 2020Material Disintegration; Material Disintegration
ALLEGEDLY, PATIENT UNDERWENT A LEFT TOTAL HIP REVISION DUE TO ELEVATED LEVELS OF CHROMIUM AND COBALT IONS IN HER BLOOD. FEMORAL HEAD AND THE FEMORAL STEM WERE REPLACED. THE ORIGINAL PROSTHESIS IMPLANTED WAS CORRODED AROUND THE NECK AND FEMORAL STEM.
Patient problems: No Information
MAUDE report 10659825 ↗InjuryNov 21, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED FROM A TOTAL HIP DUE TO A PSUEDO-TUMOR.
Patient problems: Reaction
MAUDE report 9354737 ↗
Other Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented devices
- PINNACLE 1217-25-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED735 reports
- NA 1365-52-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED683 reports
- APEX 1246-03-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 deaths613 reports
- PINNACLE 1217-20-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 deaths590 reports
- PINNACLE 1217-30-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 death484 reports
- NA 1365-53-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED404 reports
- PINNACLE ALTRX 1221-36-054Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED388 reports
- PINNACLE ALTRX 1221-32-050Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED386 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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