Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner… — Class II medical device recall Z-0386-2013
Terminated recall by Zimmer, Inc., reported 2012-11-28, distributed nationwide. Trilogy Longevity Constrained Liner devices were packaged in incorrect cartons. The product is packaged in the
| Recall number | Z-0386-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2012-08-27 |
| Classified | 2012-11-20 |
| Reported by FDA | 2012-11-28 |
| Terminated | 2013-08-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | GB |
| Quantity | 1 |
| Reason classes | labeling |
| Lot numbers | 62023769 |
| Model numbers | 00-6334-062-36 |
Product
Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves as the articular surface for a femoral head in total hip arthroplasty.
Reason for recall
Trilogy Longevity Constrained Liner devices were packaged in incorrect cartons. The product is packaged in the incorrect carton. Product labels and patient labels are correct, matching the product inside the carton.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0386-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.