LineageRecalls & reported problems across all models
Microport Orthopedics Inc. · 35 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 67
- Deaths reported
- 0
- Injuries reported
- 67
- Recalls
- 0
We found 35 models of Lineage by Microport Orthopedics Inc. in the FDA's device registry (GUDID). Together they are named in 67 adverse event reports in the FDA's MAUDE database, received between Sep 26, 2019 and Mar 23, 2026 — classified as 67 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (25 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Lineage problems
Device problems
- Insufficient Device Problem Information25
- Device Dislodged or Dislocated10
- Loss of Osseointegration6
- Break5
- Naturally Worn5
- Appropriate Device Problem Term/Code Not Available4
- Material Disintegration3
- Noise, Audible3
Patient problems
- Pain18
- Insufficient Information10
- No Information8
- Metal Related Pathology7
- Osteolysis6
- Unspecified Infection5
- Loss of Range of Motion4
- Unequal Limb Length4
Lineage models
35 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Lineage 26010008Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented7 reports
- Lineage 26000005Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented4 reports
- Lineage 26012802Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented4 reports
- Lineage 36452801Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented4 reports
- Lineage 26000011Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented3 reports
- Lineage 26010010Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented3 reports
- Lineage 26012804Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented3 reports
- Lineage 36430052Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented3 reports
- Lineage 20070053PUNCH, FEMORAL NECK2 reports
- Lineage 26000004Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented2 reports
- Lineage 26000008Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented2 reports
- Lineage 26000014Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented2 reports
- Lineage 26010009Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented2 reports
- Lineage 26012805Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 reports
- Lineage 364132X2Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 reports
- Lineage 36430056Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented2 reports
- Lineage 72003252Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented2 reports
- Lineage 20070052PUNCH, FEMORAL NECK1 report
- Lineage 20070057INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- Lineage 26000009Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented1 report
- Lineage 26000010Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented1 report
- Lineage 26010002Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented1 report
- Lineage 26010007Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented1 report
- Lineage 36430042Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented1 report
- Lineage 36430046Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented1 report
- Lineage 36430048Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented1 report
- Lineage 36430058Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented1 report
- Lineage 36450048Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented1 report
- Lineage 36450054Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented1 report
- Lineage 36450056Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented1 report
- Lineage 36452200Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented1 report
- Lineage 36452802Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented1 report
- Lineage 36453202Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented1 report
- Lineage 364532X2Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- Lineage 73003258Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented1 report
Recent Lineage adverse event reports
The 15 most recent reports across all models, 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 ↗InjuryNov 24, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, CLAIMANT (B)(6) ALLEGES THAT HE WAS IMPLANTED WITH A PHAC1212 PROFEMUR PLUS COCR MODULAR NECK (SHORT) AND A PHA00238 PROFEMUR Z FEMORAL STEM (SIZE 4) IN HIS LEFT HIP ON OR ABOUT (B)(6) 2017, IN (B)(6). IT APPEARS THAT THE IMPLANTED CUP AND LINER WERE STRYKER PRODUCTS. CLAIMANT FURTHER ALLEGES THAT HIS COBALT LEVEL MEASURED 11.6 (RESULTS DATED (B)(6) 2024) AND THAT HE WAS REFERRED TO DR. (B)(6) WHO RECOMMENDED REVISION SURGERY GIVEN CLAIMANTS SEVERELY ELEVATED METAL ION LEVELS AS WELL AS SEVERE PAIN. CLAIMANT ALLEGEDLY UNDERWENT A REVISION SURGERY ON (B)(6) 2025, AT (B)(6) HOSPITAL (REPLACEMENT COMPONENTS WERE STRYKER COMPONENTS). THE REVISION OPERATIVE NOTE STATES THAT THERE WAS TRUNNIONS AND CORROSION AT THE JUNCTION OF THE FEMORAL NECK AND COMPONENT AND THAT THE SURGEON NOTICED A FRACTURE UPON REMOVAL OF THE FEMORAL STEM, WHICH REQUIRED THE IMPLANTATION OF MULTIPLE CABLES TO FIX THE FRACTURE IN A NEAR ANATOMIC POSITION.
Patient problems: Metal Related Pathology
MAUDE report 23633133 ↗InjuryMay 21, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, THE PATIENT UNDERWENT THR IN 2009. REVISED ON (B)(6) 2025 DUE TO A PERI-PROSTHETIC FRACTURE SUSTAINED AFTER A FALL. MPO'S FEMORAL COMPONENTS REVISED WITH ANOTHER MANUFACTURER'S LONG STEM AND HEAD. (B)(4).
Patient problems: Bone Fracture(s)
MAUDE report 22062175 ↗InjuryMay 7, 2025Naturally Worn; Naturally Worn
ALLEGEDLY, THE DOCTOR REPORTS THAT THE PATIENT HAS EVIDENCE OF EARLY POLYETHYLENE WEAR; HE HAS NOT YET SCHEDULED REMOVAL OF THE MATERIAL. RELATED MPO PRODUCTS: PRODUCT ID: 36430046 LINEAGE® ACETABULAR SHELL 46MM QUAD HEMI FLARE STD GROUP 1/ LOT NO.: 16453831657950/ QTY: 1 PRODUCT ID: 26012802 COCR FEMORAL HEAD 28MM SLT TAPER +0MM NECK/ LOT NO.: 1694225/ QTY: 1 PRODUCT ID: 18080301 CANCELLOUS 6.5MM SELF-TAPPING BONE SCREW 2.0CM LENGTH/ LOT NO.: 1718278/ QTY: 1 PRODUCT ID: 18080301 CANCELLOUS 6.5MM SELF-TAPPING BONE SCREW 2.0CM LENGTH/ LOT NO.: 1711513/ QTY: 1 PRODUCT ID: PHA0CLS3 PROFEMUR® Z CLASSIC STEM SZ 3 STRAIGHT SHORT NECK/ LOT NO.: 1737747/ QTY: 1.
Patient problems: Insufficient Information
MAUDE report 21978197 ↗InjuryApr 30, 2025Naturally Worn; Naturally Worn
ALLEGEDLY, THE DOCTOR REPORTS THAT THE PATIENT HAS EARLY POLYETHYLENE WEAR AND OSTEOLYSIS OF THE FEMUR.
Patient problems: Osteolysis
MAUDE report 21938779 ↗InjuryNov 14, 2024Detachment of Device or Device Component; Device Dislodged or Dislocated; Detachment of Device or Device Component; Device Dislodged or Dislocated
ALLEGEDLY, A PATIENT WAS SEEN AT HOME AFTER HEARING A STRANGE NOISE WHILE STANDING ON THE TABLE WITH BOTH HANDS ON THE TABLE AND CROUCHING DOWN ON A CHAIR. REVISION SURGERY WAS PERFORMED DUE TO DISLOCATION OF THE BIPOLAR CUP ON X-RAY. INTRAOPERATIVE FINDINGS SHOWED THAT THE RING WAS DISLODGED AND THE CUP WAS DISLODGED. THE PATIENT WAS ASKED TO INVESTIGATE WHY THE RING WAS DISLODGED. SURGERY WAS COMPLETED WITH REPLACEMENT OF THE HEAD AND BIPOLAR CUP. (B)(4).
Patient problems: Insufficient Information
MAUDE report 20686694 ↗InjuryJun 21, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, PATIENT WAS REVISED DUE TO DISLOCATION/SUBLUXATION. SRNJR NUMBER: (B)(6). SIDE: L . GENDER: F . NON REVISED PRODUCTS: PRODUCT ID: PHA01214, PROFEMUR® NECK A/R VAR/VAL 2 LONG/, LOT NO.: 050U016270101/, QTY: (B)(4).
Patient problems: Insufficient Information
MAUDE report 19589571 ↗InjuryJun 21, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT IS GOING THROUGH PAIN AND WAS ADVISED IT COULD BE TOXICITY PAIN PERHAPS DUE TO THE METALS/METALS IN THE IMPLANTS SHE HAS.
Patient problems: Pain
MAUDE report 19581263 ↗InjuryFeb 28, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, LYSIS ? SOCKET/ADVERSE SOFT TISSUE REACTION TO PARTICULATE DEBRIS SIDE: R REVISION NJR: (B)(4). GENDER: F EXPLANTED: ACETABULAR CUP, MODULAR HEAD, ACETABULAR LINER
Patient problems: Metal Related Pathology; Osteolysis
MAUDE report 18796626 ↗InjuryFeb 27, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, DISLOCATION/SUBLUXATION/UNEXPLAINED PAIN/OTHER SIDE: R; REVISION NJR: 2184492; GENDER: F; EXPLANTED: FEMORAL STEM, ACETABULAR CUP.
Patient problems: Pain
MAUDE report 18793225 ↗InjuryFeb 8, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, INTRA-ARTICULAR METALLOSIS SECONDARY TO TRUNNION WEAR, OSTEOLYSIS, PSEUDOTUMOR AND PROXIMAL PERI-PROSTHETIC FRACTURE.
Patient problems: Metal Related Pathology; Osteolysis
MAUDE report 18673317 ↗InjuryFeb 8, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, INTRA-ARTICULAR METALLOSIS SECONDARY TO TRUNNION WEAR, OSTEOLYSIS, PSEUDOTUMOR AND PROXIMAL PERI-PROSTHETIC FRACTURE.
Patient problems: Metal Related Pathology; Osteolysis
MAUDE report 18673233 ↗InjuryApr 26, 2023Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
ALLEGEDLY, INNER SEAL OF PRODUCT NOT SEALED/NOT STERILE. PRODUCT USED.
Patient problems: Insufficient Information
MAUDE report 16815748 ↗InjuryApr 26, 2023Packaging Problem; Packaging Problem
ALLEGEDLY, INNER PACKAGE WAS NOT SEALED. PRODUCT WAS USED.
Patient problems: Insufficient Information
MAUDE report 16815503 ↗InjuryDec 22, 2022Loss of Osseointegration; Malposition of Device; Naturally Worn; Loss of Osseointegration; Malposition of Device; Naturally Worn
ALLEGEDLY, PATIENT WAS REVISED DUE TO LOOSENING - SOCKET/LYSIS-SOCKET/MALALIGNMENT-SOCKET/WEAR OF ACETABULAR COMPONENT REVISION NJR NUMBER: (B)(4). SIDE:L. PRIMARY ASA: P2 - MILD DISEASE NOT INCAPACITATING. PRODUCTS NO REVISED: PRODUCT ID: PHA05506, LOT: 89904172, QTY: 1. PRODUCT ID: PHA01204, LOT: 99926678, QTY: 1.
Patient problems: Osteolysis
MAUDE report 16035142 ↗
Other Microport Orthopedics Inc. products
All Microport Orthopedics Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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