Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Dynasty Liners: REF DLCOGA28 Recalled by MicroPort Orthopedics Inc. Due to Revision rate trends from within the MicroPort Orthopedics...

Date: June 21, 2016
Company: MicroPort Orthopedics Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact MicroPort Orthopedics Inc. directly.

Affected Products

Dynasty Liners: REF DLCOGA28, REF DLCOGB32, REF DLCOGC36, REF DLCOGD38, REF DLCOGE40, REF DLCOGF42, REF DLCOGG44, REF DLCOGH48, REF DLCOGJ52, REF DLCOGK56, For use with the conserve metal head

Quantity: 6,250 units

Why Was This Recalled?

Revision rate trends from within the MicroPort Orthopedics Inc. database evaluated for the modular head Metal on Metal THA systems show an increasing overall trend from 2009 to present and it was found that there was a specific hazard/harm for suspected tissue reaction to metal debris over one percent for modular head CONSERVE(R) systems and DYNASTY(R) metal acetabular liner systems.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About MicroPort Orthopedics Inc.

MicroPort Orthopedics Inc. has 30 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report