← FDA ENFORCEMENT
Z-2461-2026Class II

Howmedica Osteonics Corp.

Recalling firm
Howmedica Osteonics Corp.
Product type
Device
Status
Ongoing
Report date
2026-06-24
Distribution
US Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV.
Firm state
NJ
Product quantity
7 units
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
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).

Product description

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

Code / lot info

Part Number: 5521-B-300. UDI: (01)07613327026313(17)260921(10) UZD9IB. Lot Number: UZD9IB.

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.