FDA Device recall Z-0773-2013
Trilogy Acetabular Shell with Cluster Holes
- FDA Device
- Class II
- terminated
- Published 2013-02-13
On 2013-02-13 the FDA classified a Class II recall of Trilogy Acetabular Shell with Cluster 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-0773-2013 |
| 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 Shell with Cluster 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 | 00369733 00369629 61216911 61750773 61770610 61734420 61880355 61941709 61687733 61076227 61489318 61716316…00369733 00369629 61216911 61750773 61770610 61734420 61880355 61941709 61687733 61076227 61489318 61716316 61825784 62063923 61215851 61216909 61263156 61483182 61655830 61709193 61825783 61855188 61957104 61580848 61943340 62065253 62076915 61215855 61655829 61655831 61783469 61873616 61883392 61883393 61964702 61978754 61439036 61911394 62052806 61957102 61215850 61263155 61374949 61511679 61536418 61665446 61716314 61734423 61768199 61783470 61801116 61860445 61864074 61864075 61916323 61938318 61991357 61435495 62010623 61967998 62063924 61216912 61256547 61310909 61483181 61528587 61580847 61580856 61655832 61665445 61673515 61687736 61687737 61687738 61709191 61709195 61744559 61750775 61783468 61794947 61817467 61825786 61846496 61936095 61941382 61999744 61999746 62065252 61237816 61846498 61911393 62052805 61066740 61237813 61237818 61237819 61246512 61246513 61281211 61292688 |
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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-0773-2013%22
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