FreshRecalls

⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a very recent recall may be missing. Everything shown is accurate as of the last checked time on this page — for anything time-critical, confirm with the official sources linked below.

FDAClass II · Medical device · Recalled June 24, 2026

TRI TS BASEPLATE SIZE 3 recall — Howmedica Osteonics Corp.

Hazard: 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).

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID
Z-2461-2026
Brand
Howmedica Osteonics
Classification
Class II
Units affected
7 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Description

TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.

Affected products

Companies & origin

Recalling firm location
Mahwah, NJ, United States
Firm address
325 Corporate Dr, 07430-2006

Identifying details (verbatim from the notice)

Product codes / lots
Part Number: 5521-B-300. UDI: (01)07613327026313(17)260921(10) UZD9IB. Lot Number: UZD9IB.
Distribution
US Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV.
Firm notified the public via
Letter
FDA event ID
99080
Recall initiated
May 19, 2026
FDA classified
June 17, 2026
FDA report date
June 24, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.

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