FDA Device recall Z-0775-2013
Trilogy Acetabular Shells with Holes
- FDA Device
- Class II
- terminated
- Published 2013-02-13
On 2013-02-13 the FDA classified a Class II recall of Trilogy Acetabular Shells with Holes by Zimmer, citing some units of Trilogy shells manufactured since March 2009 may be below the lower range of the pore size specification (as low as 28% vs. 30% porosity specification). On 10/31/201….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0775-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-09-14 |
| Published | 2013-02-13 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Zimmer |
| Distribution | US |
Product
Trilogy Acetabular Shells with Holes. The Trilogy Acetabular System is indicated for either cemented or uncemented use in individuals undergoing surgery for rehabilitating hip damage.
Reason
Some units of Trilogy shells manufactured since March 2009 may be below the lower range of the pore size specification (as low as 28% vs. 30% porosity specification). On 10/31/2012, the firm expanded the recall action to include lots of Uni-Hole Trilogy Acetabular System shells.
Identifiers
| code_info | 61567730 61558081 61611792 61559843 61567731 61611793 61215883 00369728 00369696 61930401 61459870 61611794…61567730 61558081 61611792 61559843 61567731 61611793 61215883 00369728 00369696 61930401 61459870 61611794 61564135 61201896 61292658 61783434 61915194 00369729 00369680 61921675 61638695 61915195 61906180 61808994 61425796 61580824 61471012 61263144 61201897 00369730 00370028 00370201 00370605 00370449 00369628 61996704 61779026 61533558 61758219 61455810 61452211 61911378 61596869 61734419 61783435 61794928 61201845 61783436 62055820 61580825 61825846 62022693 61580826 61638696 61889255 61263146 61281167 61321048 61329084 61471011 61638699 61896724 61921677 61283615 61309774 61215878 61216899 61638698 61855181 61906445 62052789 61374925 61638697 61199815 61199814 61403503 61412019 61486653 61521911 61533559 61580827 61633747 61817461 61921676 61957085 61263145 61412020 61470969 61486654 61809006 61292660 61237662 61374926 61452210 61528582 61837767 61873598 61930403 61945055 62006515 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0775-2013%22
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