FDA Device recall Z-2810-2015
Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component
- FDA Device
- Class II
- terminated
- Published 2015-09-30
On 2015-09-30 the FDA classified a Class II recall of Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component by Stryker Howmedica Osteonics, citing 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 we….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2810-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-06-25 |
| Published | 2015-09-30 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Stryker Howmedica Osteonics |
| Distribution | WI |
Product
Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component
Reason
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.
Identifiers
| code_info | Lot Code 3Y0KHP |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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All Stryker Howmedica Osteonics recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2810-2015%22
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