Trinity Acetabular Shell Product Usage Total Hip Replacement — Class II medical device recall Z-1528-2016
Terminated recall by Corin USA Limited, reported 2016-05-04, distributed nationwide. Potential for abrasion of the sterile barrier pouches of the new packaging system.
| Recall number | Z-1528-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Corin USA Limited, Tampa, FL, United States |
| Recall initiated | 2016-01-29 |
| Classified | 2016-04-22 |
| Reported by FDA | 2016-05-04 |
| Terminated | 2019-12-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BE, DE, EG, GB, GH, IT, JP, PL, ZA |
| Quantity | 629 devices |
| Reason classes | sterility |
| Lot numbers | 320026, 322396, 322403, 322971, 322977, 322984, 322985, 322986, 323743, 323744, 323750 |
Product
Trinity Acetabular Shell Product Usage Total Hip Replacement.
Reason for recall
Potential for abrasion of the sterile barrier pouches of the new packaging system.
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-1528-2016. 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.