FDAJune 21, 2016device

Lineage Shell: REF 36693646, REF 36693848, REF 36694050, REF 36694252, REF 36694454, REF 36694656, REF 36694858, REF 36695060, REF 36695262, REF 36695464 For use with the conserve metal head

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

microport orthopedicsmicroport

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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