Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant… — Class II medical device recall Z-2810-2015
Terminated recall by Stryker Howmedica Osteonics Corp., reported 2015-09-30, distributed in WI. it was discovered that item 623-10-36I Lot 3Y0KHP, although meeting all device specifications, was determined
| Recall number | Z-2810-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Howmedica Osteonics Corp., Mahwah, NJ, United States |
| Recall initiated | 2015-06-25 |
| Classified | 2015-09-23 |
| Reported by FDA | 2015-09-30 |
| Terminated | 2017-08-30 |
| Distributed | WI |
| Quantity | 16 units |
| Lot numbers | 3Y0KHP |
| Model numbers | 623-10-36I |
Product
Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component
Reason for recall
it was discovered that item 623-10-36I Lot 3Y0KHP, although meeting all device specifications, was determined to be unacceptable due to a documentation issue. However the parts were inadvertently shipped to the field.
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-2810-2015. 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.