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Home › FDA recalls › TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.
CLASS II · ModerateFDA

Howmedica Osteonics Corp. recalls TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.

📅 May 19, 2026 · 📍 Nationwide
Recalling company
Howmedica Osteonics Corp.
Product
TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.
Reason
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).
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
May 19, 2026
Reported
Jun 24, 2026
Distribution
US Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV.
Status
Ongoing
Quantity
7 units
Lot / codes
Part Number: 5521-B-400. UDI: (01)07613327026061(17)260921(10) TYX7OB. Lot Number: TYX7OB.
Company location
Mahwah, NJ
Recall type
Voluntary: Firm initiated
Recall number
Z-2462-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2462-2026 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.