Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
USTAR II Knee System : Cemented Curved Stem Recalled by United Orthopedic Corporation Due to Their is a potential that the implant curved...
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 United Orthopedic Corporation directly.
Affected Products
USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: PE25153109 - PE25151109 - 9x125mm, PE25151111 - 11X125, PE25151113 - 13X125mm, PE25151115 - 15X125mm, PE25151117 - 17X125mm, PE25151119 - 19X125mm, PE25151209 - 9X150mm, PE25151211 - 11X150, PE25151213 - 13X150mm, PE25151215 - 15X150mm, PE25151217 - 17X150mm, PE25151415 - 15x200mm
Why Was This Recalled?
Their is a potential that the implant curved stem may be oriented incorrectly.
Where Was This Sold?
This product was distributed to 9 states: CA, CO, FL, IN, KY, MI, NV, TN, TX
About United Orthopedic Corporation
United Orthopedic Corporation has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report