Dynasty DSPCGE54Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI M684DSPCGE541), received between May 31, 2019 and Jul 15, 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

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryJul 15, 2021Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, PATIENT WAS REVISED DO TO UNKNOWN REASONS, AFTER A LEFT HIP ARTHROPLASTY.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 12175612 ↗
• InjuryMay 5, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

  ALLEGEDLY, PATIENT WAS REVISED DUE TO DISLOCATED LINER. COMPONENTS NOT REVISED: PROFEMUR® RENAISSANCE® STEM REDUCED SZ 14 PRODUCT ID: PLS0R414, LOT ID: 1750310. CONSERVE® TOTAL MEDIUM NECK SLEEVE PRODUCT ID: 38NS0000, LOT ID: 1723377. PROFEMUR® NECK VAR/VAL 8DG SHORT COBALT CHROME PRODUCT ID: PHAC1252, LOT ID: 1736349.

  Patient problems: No Information

  MAUDE report 10027010 ↗
• 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: No Information

  MAUDE report 9354114 ↗
• InjuryMay 31, 2019Malposition of Device; Malposition of Device

  ALLEGEDLY, PATIENT UNDERWENT RIGHT THR ON (B)(6) 2018, REVISED ON (B)(6) 2019 DUE TO CUP MALALIGNMENT AND STEM SUBSIDENCE. SURGEON REPORTED CHOICE OF STEM SIZE AS THE CAUSE. THE CUP WAS REPLACED ALONG WITH A LATERALIZED LINER, BOTH COMPETITOR'S PRODUCTS. THE HEAD WAS ALSO REVISED WITH MICROPORT'S COMPONENT.

  Patient problems: No Information

  MAUDE report 8660529 ↗