Dynasty DLXPLE36Recalls & reported problems
Microport Orthopedics Inc. · DYNASTY® A-CLASS® 15 DG POLY LINER 36MM GROUP E · Class 2 · Implant
All models of Dynasty (44)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M684DLXPLE361), received between Nov 21, 2019 and Apr 5, 2023 — classified as 2 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
- Noise, Audible1
Patient problems
- Pain2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 5, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
ALLEGEDLY, PLAINTIFF UNDERWENT A RIGHT-SIDED REVISION OF THE ACETABULAR LINER/FEMORAL HEAD AND NECK. THE PROFEMUR TOTAL HIP SYSTEM HAS FAILED DUE TO CORROSION RELATED ADVERSE TISSUE REACTIONS AND THE DEVICE HAS BEEN SURGICALLY REMOVED, PLAINTIFF PRESENTED PAIN AND DISASSOCIATION OF THE ACETABULAR POLUETHYLENE COMPONENT WITHOUT DISLOCATION, MODULAR HEAD (PHAC1202) AND COBALT CHROME HEAD (26000025) WERE IMPLANTED. PRODUCTS NOT REVISED: PRODUCT ID: 18080303, CANCELLOUS SELF-TAPPING 6.5MM BONE SCREW 3.0CM LENGTH, LOT: 1558083, QTY: 1 PRODUCT ID: PPW38372, PROFEMUR® 115MM STRAIGHT FULLY COATED CYL/PS SZ 12, LOT: 1571390, QTY: 1 PRODUCT ID: PPW38354, "PROFEMUR® R" PROX BODY PLASMA SPRAY X-SMALL MODULAR LOT: 1562181, QTY: 1 PRODUCT ID: DSBFGE54, DYNASTY® BF SHELL 54MM GROUP E LOT: 1565510, QTY: 1 PRODUCT ID: 18080303, CANCELLOUS SELF-TAPPING 6.5MM BONE SCREW 3.0CM LENGTH LOT: 1558084, QTY: 1.
Patient problems: Pain
MAUDE report 16683362 ↗InjuryNov 21, 2019Detachment of Device or Device Component; Noise, Audible; Detachment of Device or Device Component; Noise, Audible
ALLEGEDLY PATIENT PRESENTED WITH PAIN AND SQUEAKING SOUNDS, UPON X-RAY THE LINER SHOWED DISASSOCIATION. ALL MPO IMPLANTS WERE EXPLANTED AND REPLACED WITH ANOTHER MANUFACTURERS SYSTEM, APART FROM THE FEMORAL STEM. (B)(4).
Patient problems: Pain
MAUDE report 9353986 ↗
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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