Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Prosthesis Recalled by Howmedica Osteonics Corp. Due to Stryker has discovered that the internal profile of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Howmedica Osteonics Corp. directly.
Affected Products
Prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer.
Quantity: 11 devices
Why Was This Recalled?
Stryker has discovered that the internal profile of the Triathlon Tritanium Tibial Component (Baseplate), size 4, is potentially oversized. Due to a manufacturing issue in Lot Number CTD44301, there may be a witness mark (taper) at the bottom of the internal profile of the baseplate. The taper prevents the insert from locking on the baseplate.
Where Was This Sold?
This product was distributed to 13 states: AZ, GA, MA, MI, MN, NH, NJ, OR, PA, SC, UT, WA, WV
About Howmedica Osteonics Corp.
Howmedica Osteonics Corp. has 229 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report