TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.
FDA Recall Z-2461-2026 · Posted 2026-06-17
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Recalling FirmHowmedica Osteonics Corp.
Recall StatusOpen, Classified
Product CodeMBH
Date Initiated2026-05-19
Product Quantity7 units
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).
Firm Action
Stryker notified consignees on about 05/19/2026 via letter sent using FedEx 2-day service. Consignees were instructed to inform users of the Urgent Medical Device Recall and forward the notice to all individuals who need to be made aware or organizations who have consigned product, immediately check all stock areas and/or operating room storage to determine if any devices from the affected product list are on hand, and complete and return the provided Urgent Medical Device Recall Business Reply Form.
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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