DynastyRecalls & reported problems across all models
Microport Orthopedics Inc. · 44 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 149
- Deaths reported
- 0
- Injuries reported
- 149
- Recalls
- 0
We found 44 models of Dynasty by Microport Orthopedics Inc. in the FDA's device registry (GUDID). Together they are named in 149 adverse event reports in the FDA's MAUDE database, received between May 20, 2019 and Apr 13, 2026 — classified as 149 injuries.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (41 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 Dynasty problems
Device problems
- Detachment of Device or Device Component41
- Insufficient Device Problem Information33
- Device Dislodged or Dislocated32
- Loss of Osseointegration21
- Naturally Worn18
- Break7
- Malposition of Device7
- Noise, Audible7
Patient problems
- No Information40
- Pain38
- Insufficient Information28
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available13
- Metal Related Pathology9
- Loss of Range of Motion8
- Unspecified Infection7
- Failure of Implant4
Dynasty models
44 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Dynasty DLXPGD36Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented19 reports
- Dynasty DSBFGD52Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)12 reports
- Dynasty DLXPGE38Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented7 reports
- Dynasty DLXPLD36Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous7 reports
- Dynasty DSBFGE54Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)7 reports
- Dynasty DBFPGD52Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented5 reports
- Dynasty DLXPGG42Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented5 reports
- Dynasty DLXPLF40Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous5 reports
- Dynasty DSBFGF56Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)5 reports
- Dynasty DLXPGE36Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented4 reports
- Dynasty DLXPGF40Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous4 reports
- Dynasty DLXPGG36Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented4 reports
- Dynasty DLXPLE38Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented4 reports
- Dynasty DLXPLG36Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous4 reports
- Dynasty DSPCGB48Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented4 reports
- Dynasty DSPCGD52Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented4 reports
- Dynasty DSPCGE54Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous4 reports
- Dynasty DSPCGF56Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented4 reports
- Dynasty DLXPGB28Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented3 reports
- Dynasty DLXPGC32Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented3 reports
- Dynasty DLXPLG42Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented3 reports
- Dynasty DBFPGE54Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous2 reports
- Dynasty DBFPGG58Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous2 reports
- Dynasty DLXPGF36Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented2 reports
- Dynasty DLXPLE36Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous2 reports
- Dynasty DLXPLF36Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 reports
- Dynasty DSBFGC50Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)2 reports
- Dynasty DSBFGG58Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)2 reports
- Dynasty DSPCGB46Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented2 reports
- Dynasty DSPCGG58Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous2 reports
- Dynasty DLDMGC38Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 report
- Dynasty DMNE2838Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 report
- DYNASTY® 33330010IMPACTOR1 report
- Dynasty DBFPGF56Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented1 report
- Dynasty DBFPGG60Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented1 report
- Dynasty DBFRGC50Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous1 report
- Dynasty DBFRGE54Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous1 report
- Dynasty DBFRGG58Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous1 report
- Dynasty DLXPGH46Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented1 report
- Dynasty DLXPLC32Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented1 report
- Dynasty DLXPLD32Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented1 report
- Dynasty DLXPLF32Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous1 report
- Dynasty DSBFGB48Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)1 report
- Dynasty DSPCGC50Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous1 report
Recent Dynasty adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryApr 13, 2026Loss of Osseointegration
ALLEGEDLY, LINER AND HEAD REVISED. STEM AND CUP RETAINED. CUP WAS VERTICAL. JOINT WAS NOT TIGHT AND HEAD WAS RIDING ON POLY SUPERIOR EDGE CAUSING POLY TO FRACTURE. LINER WAS NOT DISASSOCIATED. XRAYS TO BE PROVIDED. REVISED TO DUAL MOBILITY, ADDING 9-10MM OF LENGTH TO STABILIZE AND TIGHTEN JOINT. NON REVISED RELATED MPO PRODUCTS: PROFEMUR® PRESERVE CLASSIC /PRODUCT ID: PPRCLS06 /LOT. NO: 1787281 /QTY: 1. ADDITIONAL INFORMATION RECEIVED ON 03/18/2026 BY RELIABILITY ENGINEERING CONFIRMING CUP LOOSENING. THIS COMPONENT WAS NOT REVISED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24865139 ↗InjuryFeb 23, 2026Break; Malposition of Device; Naturally Worn
ALLEGEDLY, LINER AND HEAD REVISED. STEM AND CUP RETAINED. CUP WAS VERTICAL. JOINT WAS NOT TIGHT AND HEAD WAS RIDING ON POLY SUPERIOR EDGE CAUSING POLY TO FRACTURE. LINER WAS NOT DISASSOCIATED. XRAYS TO BEPROVIDED. REVISED TO DUAL MOBILITY, ADDING 9-10MM OF LENGTH TO STABILIZE AND TIGHTEN JOINT. NON REVISED RELATED MPO PRODUCTS: PROFEMUR® PRESERVE CLASSIC /PRODUCT ID: PPRCLS06 /LOT. NO: 1787281 /QTY: 1. DYNASTY® BF SHELL PRIMARY /PRODUCT ID: DBFPGE54 /LOT. NO: 1821927 /QTY: 1.
Patient problems: Failure of Implant; Insufficient Information
MAUDE report 24415848 ↗InjuryDec 10, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
ALLEGEDLY, LINER WORE THROUGH/BECAME DISASSOCIATED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23767334 ↗InjuryDec 5, 2025Loss of Osseointegration; Loss of Osseointegration
ALLEGEDLY, ACETABULAR SHELL APPEARED LOOSE ON X-RAY. ADDITIONAL INFORMATION RECEIVED ON 11/13/2025: THE CUP WAS EXPLANTED AND REPLACED WITH A DEPUY CUP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23727954 ↗InjuryDec 2, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT HAD A MOD Z STEM & NECK, DYNASTY METAL ON METAL ACETABULUM. SURGEON WANTED TO REMOVE THE METAL ON METAL (MOM) INCLUDING THE STEM. HE RETAINED THE DYNASTY SHELL. INSERTED A DUAL MOBILITY LINER AND INSERT. HE REPLACED THE STEM WITH A ZIMMER REVISION STEM AND 28MM CERAMIC HEAD.
Patient problems: Insufficient Information; Metal Related Pathology
MAUDE report 23697522 ↗InjurySep 5, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, A PATIENT WITH BMI OVER 40 AND HAS ADVISED LEGAL THAT BROUGHT SURGEON TO FOLLOW UP WITH HOSPITAL.
Patient problems: Insufficient Information
MAUDE report 22984224 ↗InjuryApr 30, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, THE PATIENT UNDERWENT L THR ON (B)(6) 2020. REVISED ON (B)(6) 2020 DUE TO METALLOSIS. FEMORAL HEAD REVISED WITH ANOTHER MPO HEAD, SHELL AND LINER REVISED WITH ANOTHER MANUFACTURER'S ACETABULAR COMPONENTS. REF (B)(4). NON-MPO DEVICES: 1. ACETABULAR INSERT REF: (B)(4). 2. ACETABULAR SHELL REF: (B)(4).
Patient problems: Metal Related Pathology
MAUDE report 21939892 ↗InjuryApr 3, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, ON (B)(6) 2024 THE PATIENT REPORTED COMPLICATIONS FROM THE REVISION DEVICES. SECOND REVISION SURGERY EXPECTED. NO OTHER INFORMATION AVAILABLE.
Patient problems: Insufficient Information
MAUDE report 21769684 ↗InjuryDec 26, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT UNDERWENT THR ON (B)(6) 2019. REVISED ON (B)(6) 2024 DUE TO AN INFECTION. WASHOUT PERFORMED, HEAD AND LINER REPLACED. (B)(6).
Patient problems: Unspecified Infection
MAUDE report 21021607 ↗InjuryNov 1, 2024Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component
ALLEGEDLY, DURING REVISION OF A PATIENT WITH A THA REPLACEMENT IN 2011, A LINER AND NECK FRACTURE WERE IDENTIFIED. THE NECK WAS CONFIRMED ON PREOPERATIVE CT AND THE LINER WAS FOUND TO HAVE BEEN DAMAGED INTRAOPERATIVELY. THE LINER WAS DAMAGED BECAUSE IT PROTRUDED FROM THE CUP. AS FOR THE NECK, IT IS NECESSARY TO INVESTIGATE THE POSSIBILITY OF INTERNAL DAMAGE. JAPAN (B)(4).
Patient problems: Insufficient Information
MAUDE report 20587971 ↗InjurySep 26, 2024Naturally Worn; Naturally Worn
ALLEGEDLY, THE DEVICES FAILED DUE TO CORROSION OF THE MODULAR NECK AT THE HEAD-NECK JUNCTION AND WHERE THE NECK SEATED IN THE POCKET OF THE STEM, AND EARLY EXCESSIVE WEAR OF THE LINER. ALSO, PRODUCTION OF METAL DEBRIS RESULTING IN METALLOSIS, POLYETHYLENE WEAR DEBRIS, ADVERSE LOCAL TISSUE REACTION TO PARTICLES, WEAKNESS, AND PAIN.
Patient problems: Pain
MAUDE report 20313054 ↗InjuryAug 22, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, HIP REVISED FOR RECURRENT DISLOCATION.
Patient problems: Insufficient Information
MAUDE report 20027292 ↗InjuryJun 10, 2024Mechanical Jam; Mechanical Jam
ALLEGEDLY, DURING A PRIMARY THR THE SURGEON WAS UNABLE TO RELEASE THE PROCOTYL L CUP FROM THE IMPACTOR INSTRUMENT, EVENTUALLY HE HAD TO USE ANOTHER MANUFACTURER'S CUP AND LINER. 30 MIN DELAY CAUSED. THE REP SUSPECTS THE SURGEON CROSS THREADED THE CUP ON THE IMPACTOR.
Patient problems: Insufficient Information
MAUDE report 19498983 ↗InjuryMay 3, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, MPO DYNASTY LINER REVISED WITH THE DYNASTY LINER SOURCED IN PREPARATION FOR THE SUSPECTED INFECTION. REP DOESN?T HAVE ANY INFORMATION ON ANY OTHER COMPONENTS THAT MAY HAVE BEEN REVISED DURING THIS CASE. (B)(4).
Patient problems: Insufficient Information
MAUDE report 19239943 ↗InjuryFeb 12, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, REVISION DONE DUE TO PAINFUL HIP. THEY TOOK OUT THE STEM, NECK, HEAD AND POLY. THEY REPLACE THE POLY. PRODUCTS NO REVISE: PRODUCT: DSBFGD52 DYNASTY® BF SHELL 52MM GROUP D, LOT: 1502022, QTY: 1
Patient problems: Pain
MAUDE report 18686854 ↗
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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