Dynasty DLXPLD36Recalls & reported problems
Microport Orthopedics Inc. · DYNASTY® A-CLASS® 36MM 15DG GROUP D CROSSLINKED POLY LINER · Class 2 · Implant
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI M684DLXPLD361), received between Sep 20, 2019 and Apr 3, 2025 — classified as 7 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (4 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information4
- Detachment of Device or Device Component2
- Break1
- Loss of Osseointegration1
- Naturally Worn1
Patient problems
- Pain3
- Insufficient Information2
- No Information2
- Joint Dislocation1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
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 ↗InjuryAug 10, 2023Break; Naturally Worn; Break; Naturally Worn
ALLEGEDLY, POLYETHYLENE WEAR WITH BREAKAGE OF THE ACETABULAR SYSTEM AND METALLOSIS ON THE TROCHANTER AND THE PELVI TROCHANTERIC MUSCLES.
Patient problems: Insufficient Information
MAUDE report 17500252 ↗InjuryDec 22, 2021Loss of Osseointegration; Loss of Osseointegration
InjurySep 1, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
ALLEGEDLY, PATIENT WAS REVISED DUE TO PAIN AND POSSIBLE MOVEMENT OF CUP AND LINER. WHEN REMOVING CUP THE LINER HAD DISLODGED FROM THE CUP. ALL OTHER MPO IMPLANTS REMOVED AND REPLACED WITH A DIFFERENT MANUFACTURERS PRODUCTS. (B)(6) / C978.
Patient problems: Pain
MAUDE report 10476166 ↗InjuryJan 6, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY PATIENT WAS REVISED DUE TO UNKNOWN REASONS. LEFT HIP.
Patient problems: No Information
MAUDE report 9554855 ↗InjuryOct 23, 2019Detachment of Device or Device Component; Insufficient Device Problem Information; Detachment of Device or Device Component; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED DUE TO POLY LINER DISLOCATION.
Patient problems: Joint Dislocation; No Information
MAUDE report 9225843 ↗InjurySep 20, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT PRESENTED WITH PAIN. REMOVAL OF DYNASTY CUP FOR LOOSENING. NO ACUTE INJURY OF PATIENT. MPO IMPLANTS WERE REMOVED AND REPLACED WITH ANOTHER SUPPLIERS IMPLANTS.
Patient problems: Pain
MAUDE report 9100714 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.