Dynasty DLXPGF40Recalls & reported problems
Microport Orthopedics Inc. · DYNASTY® A-CLASS® 40MM STD GROUP F CROSSLINKED POLY LINER · Class 2 · Implant
All models of Dynasty (44)
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 M684DLXPGF401), received between Feb 13, 2020 and Jul 13, 2021 — classified as 4 injuries.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component2
- Insufficient Device Problem Information2
Patient problems
- Arthritis1
- Insufficient Information1
- 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.
InjuryJul 13, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED DO TO UNKNOWN REASONS, AFTER A RIGHT TOTAL HIP ARTHROPLASTY.
Patient problems: Insufficient Information
MAUDE report 12158449 ↗InjuryJul 22, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
ALLEGEDLY, PATIENT WAS REVISED FOR LINER DISASSOCIATION. TIME TO REVISION WAS 57 MONTHS COMPONENT NOT REVISED: DYNASTY(R) SHELL PRODUCT ID: DXXXGF56 LOT ID: NOT INDICATED. ADDITIONAL INFORMATION : INDICATION FOR SURGERY WAS OSTEOARTHRITIS. BMI: 33.
Patient problems: Arthritis
MAUDE report 10311825 ↗InjuryJul 22, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
ALLEGEDLY, PATIENT WAS REVISED FOR LINER DISSOCIATION. TIME TO REVISION WAS 91 MONTHS COMPONENTS NOT REVISED: A-CLASS(R) FEMORAL HEAD PRODUCT ID: 38XX40XX, LOT ID: NOT INDICATED. PROFEMUR(R) COCR NECK PRODUCT ID: PHAC12XX, LOT ID: NOT INDICATED. INDICATION FOR SURGERY WAS OSTEOARTHRITIS. BMI: 30.
Patient problems: No Information
MAUDE report 10307270 ↗InjuryFeb 13, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, THE DEVICE FAILED DUE TO METAL DEBRIS CORROSION AND RESULTANT METAL IONS, DUE TO THE METAL ON METAL DESIGN BETWEEN THE ARTICULATING SURFACES, CAUSING CONTINUING AND OTHERWISE IRREVERSIBLE PHYSICAL INJURY TO THE PATIENT.
Patient problems: Pain
MAUDE report 9708245 ↗
Other Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous devices
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- OXINIUM 71342340Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous32 reports
- EXETER 0580-1-351Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous29 reports
- INSTRUMENT 2101-0200Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous27 reports
- REFLECTION 71330001Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous20 reports
- Accolade 6720-0330Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous18 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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