FDA Device recall Z-0684-2017
Dynasty Liners: REF DLCOGA28, REF DLCOGB32, REF DLCOGC36, REF DLCOGD38, REF DLCOGE40, REF DLCOGF42, REF DLCOGG44, REF DLCOGH48, REF DLCOGJ5…
- FDA Device
- Class III
- terminated
- Published 2016-12-07
On 2016-12-07 the FDA classified a Class III recall of Dynasty Liners: REF DLCOGA28, REF DLCOGB32, REF DLCOGC36, REF DLCOGD38, REF DLCOGE40, REF DLCOGF42, REF DLCOGG44, REF DLCOGH48, REF DLCOGJ5… by Microport Orthopedics, citing 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 pr….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0684-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2016-06-21 |
| Published | 2016-12-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Microport Orthopedics |
| Distribution | US |
Product
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
Reason
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.
Identifiers
| code_info | Serial Numbers: REF DLCOGA28 Seral Numbers: 1509498, 1509897, 107461555, 117476083, 127477625, 0411341968, 0611341…Serial Numbers: REF DLCOGA28 Seral Numbers: 1509498, 1509897, 107461555, 117476083, 127477625, 0411341968, 0611341969, 0901199714 REF DLCOGB32 Serial Numbers: 1428321, 027403682, 027403684, 027412214, 027412216, 027412218, 027412220, 027412222, 029789268, 048571448, 058605178, 068625411, 069837383, 078628910, 079859721, 087467577, 097474918, 097476396, 097477626, 098657540, 099905615, 099927666, 0101018635, 107480309, 107486655, 109968495, 0111248666, 0111254637, 117486656, 117501983, 119982392, 127504540, 127508429, 0211298850, 0211298851, 0401072608, 0501123237, 0601150684, 0711370347, 0711370832, 0711371855, 0711388872, 0801184970, 0801185465, 0901196484, 0901199209, 0901200444, 0901200704 REF DLCOGC36 Serial Numbers: 1389336, 1411596, 1412300, 1419309, 1421706, 1421872, 1421873, 1425040, 1425041, 1426635, 1441425, 1447128, 1448009, 017395680, 017396168, 017398843, 019752394, 027406078, 027406080, 027406549, 027408437, 027408506, 027412667, 029797073,038565179, 0 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0684-2017%22
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