Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee Recalled by Howmedica Osteonics Corp. Due to Customers may receive the incorrect size implant from...
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
Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee system devices are sterile, single-use devices intended for us in revision total knee arthroplasty to alleviate pain and restore function.
Quantity: 77 total products
Why Was This Recalled?
Customers may receive the incorrect size implant from what is labeled on the box.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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