Z-2462-2026 Class II Ongoing
FDA device recall Z-2462-2026 was initiated by Howmedica Osteonics Corp. on May 19, 2026 and is designated Class II. 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… The recall status is ongoing. Affected quantity: 7 units.
Recall Details
- Product Type
- Devices
- Report Date
- June 24, 2026
- Initiation Date
- May 19, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 7 units
Product Description
TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.
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).
Distribution Pattern
US Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV.
Code Information
Part Number: 5521-B-400. UDI: (01)07613327026061(17)260921(10) TYX7OB. Lot Number: TYX7OB.