Drug recall
TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.
FDA recall event 99080 · Class II · Howmedica Osteonics Corp.
Key facts
| Event ID | 99080 |
|---|---|
| Recall numbers | Z-2461-2026, Z-2462-2026 |
| Recalling firm | Howmedica Osteonics Corp. |
| Product type | Devices |
| Products | TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300., TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | May 19, 2026 |
| Report date | Jun 24, 2026 |
| City | Mahwah |
| State | NJ |
| Country | United States |
| FEI number | 3003070421 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: