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, Non Coated for the following reference numbers: REF: PE25153109 - 9x125mm, PE25153209 - 9x150mm, PE25153113 - 13x125mm, PE25153111- 11x125mm, PE25153115 - 15x125mm, PE25153211 - 11x150mm, PE25153213 - 13x150mm, PE25153217 - 17x150mm, PE25153117 - 17x125mm, PE25153015 - 15x100mm, PE25153215 - 15x150mm
Quantity: 479 units
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