CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9 — Class II medical device recall Z-0593-2018
Terminated recall by DePuy Orthopaedics, Inc., reported 2018-02-21. Incorrect device in the package. A package that was labeled as the CORAIL COXA VARA HIGH OFFSET STEM Collared
| Recall number | Z-0593-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Orthopaedics, Inc., Warsaw, IN, United States |
| Recall initiated | 2017-07-12 |
| Classified | 2018-02-12 |
| Reported by FDA | 2018-02-21 |
| Terminated | 2019-05-20 |
| Quantity | 21 units |
| Reason classes | labeling |
| Lot numbers | 5291990 |
| Model numbers | 3L93709 |
Product
CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9
Reason for recall
Incorrect device in the package. A package that was labeled as the CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9 (Part No. 3L93709 / Lot No. 5291990), contained the CORAIL HIGH OFFSET STEM Collarless SIZE 14 (Part No. L20314 / Lot No. 5292130).
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-0593-2018. 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.