- Recalling firm
- Howmedica Osteonics Corp.
- 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).
- Affected products (lot / model / serial)
- Part Number: 5521-B-300. UDI: (01)07613327026313(17)260921(10) UZD9IB. Lot Number: UZD9IB.
- Units affected
- 7 units
- Distribution pattern
- US Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV.
- Firm location
- Mahwah, NJ, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2461-2026
- Recall initiated
- May 19, 2026
- FDA classification date
- June 17, 2026
- FDA report date
- June 24, 2026
- FDA event ID
- 99080
- Last updated on HTM Vibe
- July 23, 2026