Home/Recalls/FDA-Z-2461-2026
FDA DevicesClass II

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

Published: June 24, 2026Recall ID: Z-2461-2026Category: devicesCountry: US

Reason for Recall / Hazard

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 & Identification

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

Additional Source Details

FieldValue
CityMahwah
StateNJ
Event id99080
Address 1325 Corporate Dr
Code infoPart Number: 5521-B-300. UDI: (01)07613327026313(17)260921(10) UZD9IB. Lot Number: UZD9IB.
Postal code07430-2006
Report date20260624
Product typeDevices
Product quantity7 units
Reason for recallStryker 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).
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260519
Initial firm notificationLetter
Center classification date20260617

Overview

  • Recalling FirmHowmedica Osteonics Corp.
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV.
Official Agency Alert