TRABECULAR METAL MODULAR ACETABULAR SYSTEM — Class II medical device recall Z-1496-2014
Terminated recall by Zimmer, Inc., reported 2014-04-30, distributed nationwide. The shell was missing the locking ring.
| Recall number | Z-1496-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2014-04-01 |
| Classified | 2014-04-24 |
| Reported by FDA | 2014-04-30 |
| Terminated | 2014-09-11 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA |
| Quantity | 17 units |
| Lot numbers | 62490588 |
| Model numbers | 00-6202-060-22 |
Product
TRABECULAR METAL MODULAR ACETABULAR SYSTEM, Shell with Cluster Holes, Porous 60mm. Catalog number 00-6202-060-22; Hip implant component.
Reason for recall
The shell was missing the locking ring.
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-1496-2014. 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.