FDA Device recall Z-2462-2026
TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400
- FDA Device
- Class II
- ongoing
- Published 2026-06-24
On 2026-06-24 the FDA classified a Class II recall of TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400 by Howmedica Osteonics, citing stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlo….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2462-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-05-19 |
| Published | 2026-06-24 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Howmedica Osteonics |
| Distribution | US |
Product
TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.
Reason
Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lot UZD9IB).
Identifiers
| code_info | Part Number: 5521-B-400. UDI: (01)07613327026061(17)260921(10) TYX7OB. Lot Number: TYX7OB. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2462-2026%22
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