FDA Device recall Z-0593-2018
CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9
- FDA Device
- Class II
- terminated
- Published 2018-02-21
On 2018-02-21 the FDA classified a Class II recall of CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9 by Depuy Orthopaedics, citing 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 HIG….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0593-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-07-12 |
| Published | 2018-02-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Depuy Orthopaedics |
| Distribution | n/a |
Product
CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9
Reason
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).
Identifiers
| code_info | Part No. 3L93709 and Lot No. 5291990 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0593-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.