FDAFDA recall Z-2461-2026 · Jun 24, 2026
Howmedica Osteonics Corp.: TRI TS BASEPLATE SIZE 3 recall
Recall found
Product
TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.
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).
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Part Number: 5521-B-300. UDI: (01)07613327026313(17)260921(10) UZD9IB. Lot Number: UZD9IB.
- Quantity
- 7 units
- Distribution
- US Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV.
- Recalling firm
- Howmedica Osteonics Corp., Mahwah, NJ
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-05-19
Source: openFDA enforcement record Z-2461-2026 · search recall number Z-2461-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.