Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part Recalled by Uoc Usa Inc Due to Due to product not meeting specification for concentricity...
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 Uoc Usa Inc directly.
Affected Products
United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part, RHS, 25 mm Length, Catalog # 2915-1025
Quantity: 3 devices
Why Was This Recalled?
Due to product not meeting specification for concentricity and failing to meet requirements of dynamic fatigue testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Uoc Usa Inc
Uoc Usa Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report