CORAIL AMT STANDARD OFFSET NECK SEGMENT — Class II medical device recall Z-1127-2019
Terminated recall by DePuy Orthopaedics, Inc., reported 2019-04-17, distributed nationwide. There is the potential for debris/material to be found behind the O-rings in the neck trials.
| Recall number | Z-1127-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Orthopaedics, Inc., Warsaw, IN, United States |
| Recall initiated | 2018-09-21 |
| Classified | 2019-04-11 |
| Reported by FDA | 2019-04-17 |
| Terminated | 2020-04-22 |
| Distributed | Nationwide (US) |
| Quantity | 12,639 total |
| Lot numbers | 1212901, 1218481, 1226220, 1230761, 1230762, 1700575, 1781381, 1812714, 1812714A, 1817780, 1860264, 1865892, 1874689, 1874692, 1874695, 1885306, 1899212, 1899213, 1910187, 1979239, 2002010, 2024019, 2043428, 2078239, 2102693, 2129111, 2153317, 2153318, 2153319, 2153320, 2163174, 2249115, 2249116, 2252364, 2274452, 2275487, 2284306, 2284307, 2309644, 2309645 and 75 more |
Product
CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty.
Reason for recall
There is the potential for debris/material to be found behind the O-rings in the neck trials.
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-1127-2019. 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.