TRI TS BASEPLATE SIZE 4 — Class II medical device recall Z-2462-2026
Ongoing recall by Howmedica Osteonics Corp., reported 2026-06-24, distributed nationwide. Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging label
| Recall number | Z-2462-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Howmedica Osteonics Corp., Mahwah, NJ, United States |
| Recall initiated | 2026-05-19 |
| Classified | 2026-06-17 |
| Reported by FDA | 2026-06-24 |
| Distributed | Nationwide (US) |
| Quantity | 7 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 07613327026061 |
| Lot numbers | TYX7OB |
| Model numbers | 5521-B-400 |
Product
TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.
Reason for recall
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).
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-2462-2026. 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.