Lineage 26012802Recalls & reported problems
Microport Orthopedics Inc. · COCR FEMORAL HEAD 28MM SLT TAPER +0MM NECK · Class 2 · Implant
All models of Lineage (35)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 M684260128021), received between May 19, 2020 and May 16, 2022 — classified as 4 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.
Most reported problems
Device problems
- Device Dislodged or Dislocated2
- Detachment of Device or Device Component1
- Insufficient Device Problem Information1
- Loss of Osseointegration1
Patient problems
- Failure of Implant2
- Joint Laxity1
- No Information1
- Pain1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryMay 16, 2022Detachment of Device or Device Component; Device Dislodged or Dislocated; Detachment of Device or Device Component; Device Dislodged or Dislocated
ALLEGEDLY, THE FEMORAL HEAD DISENGAGED FROM THE BIPOLAR HEAD UNEXPECTEDLY. NON-REVISED PRODUCTS: PRODUCT ID: PHA00232, PROFEMUR® Z FEMORAL STEM S 1 CEMENT LESS/ LOT NUMBER: 1897645/ QTY. 1
Patient problems: Failure of Implant
MAUDE report 14409502 ↗InjuryMar 16, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, PATIENT WAS REVISED DUE TO DISLOCATION/SUBLUXATION. REVISION NJR NUMBER: 4489106. SIDE:L. PRIMARY ASA: P3 - INCAPACITATING SYSTEMIC DISEASE. COMPONENT NOT REVISED: PROFEMUR TL CLASSIC FIXED NECK SIZE 3 PRODUCT ID: PRTLS023 LOT NO.: 1670985. (B)(6) REFERENCE NO: (B)(4).
Patient problems: Failure of Implant; Joint Laxity
MAUDE report 11495625 ↗InjuryJul 29, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED DUE TO PAIN. REVISION NJR NUMBER: (B)(4) SIDE: R. PRIMARY ASA: P2 - MILD DISEASE NOT INCAPACITATING COMPONENTS NOT REVISED: PROFEMUR® L HIP STEM SIZE 3 HA COATED PRODUCT ID PHA05506 LOT ID 511348822. PROFEMUR® NECK 8DG A/R SHORT PRODUCT ID PHA01232 LOT ID 511357101.
Patient problems: Pain
MAUDE report 10337626 ↗InjuryMay 19, 2020Loss of Osseointegration; Loss of Osseointegration
ALLEGEDLY, REVISED DUE TO TOTAL ASEPTIC LOOSENING.
Patient problems: No Information
MAUDE report 10072228 ↗
Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented devices
- BIOLOX DELTA 1365-32-310Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented551 reports
- PINNACLE ALTRX 1221-36-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented481 reports
- BIOLOX DELTA 1365-32-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death314 reports
- BIOLOX DELTA 1365-36-720Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death189 reports
- DJO SURGICAL 400-03-362Encore Medical, L.P. · Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented187 reports
- Anthology 71365705Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented176 reports
- BIOLOX DELTA 1365-40-710Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented170 reports
- PINNACLE GRIPTION 1217-32-054Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented169 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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