Dynasty DLXPLF32Recalls & reported problems
Microport Orthopedics Inc. · DYNASTY® A-CLASS® 15DG POLY LINER 32MM GROUP F · Class 2 · Implant
All models of Dynasty (44)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M684DLXPLF321), received between Apr 14, 2021 and Apr 14, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (1 report).
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
- Inadequacy of Device Shape and/or Size1
- Malposition of Device1
Patient problems
- Loss of Range of Motion1
- Pain1
- Unequal Limb Length1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 14, 2021Inadequacy of Device Shape and/or Size; Malposition of Device
ALLEGEDLY, PATIENT UNDERWENT LEFT THR ON (B)(6) 2017 WITH A SUPERPATH TECHNIQUE. PATIENT COMPLAINING ABOUT GROIN PAIN AND SUING PRIMARY SURGEON. PRIMARY SURGEON WOULD NOT CARRY OUT A REVISION AS ALL COMPONENTS ARE WELL FIXED AND ALIGNED. PATIENT SEEKING REVISION WITH ANOTHER SURGEON. ADDITIONAL INFORMATION RECEIVED ON (B)(6) 2021 FROM DISTRIBUTOR SURGICAL SPECIALTIES: ADDING INCIDENT DESCRIPTION, DATE OF REVISION 19 MAR 2021, CONFIRMING HEAD AND STEM WERE NOT REVISED AND CUP, LINER AND SCREWS WERE REVISED WITH OTHER MANUFACTURER'S COMPONENTS. ALLEGEDLY, REVISING SURGEON REPORTED CUP MALPOSITION WITH LEG LENGTH DISCREPANCY AND IMPINGEMENT. COMPONENTS NOT REVISED: BIOLOX DELTA FEMORAL HEAD / PRODUCT ID: PHA04408 / LOT NO.: 1703553. PROFEMUR L CLASSIC FEMORAL STEM / PRODUCT ID: PHAS5506 / LOT NO.: 1697533. (B)(6)- (B)(4).
Patient problems: Loss of Range of Motion; Pain; Unequal Limb Length
MAUDE report 11668865 ↗
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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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