Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EVOLUTION MP TIBIAL BASE Recalled by Microport Orthopedics INC. Due to Some units of the EVOLUTION Tibial Base was...
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 Microport Orthopedics INC. directly.
Affected Products
EVOLUTION MP TIBIAL BASE, REF ETPKN8SR, SIZE 8 RIGHT, TYPE PRIMARY, FIT CEMENTED, STYLE KEELED, STERILE R, Rx ONLY, MicroPort Orthopedics, Inc. Knee prosthesis component.
Quantity: 17 units
Why Was This Recalled?
Some units of the EVOLUTION Tibial Base was affected by a casting tool issue which caused varying retaining wall thickness and keel offset in the finished product.
Where Was This Sold?
This product was distributed to 8 states: AL, AZ, ID, IA, KS, MO, TX, WV
About Microport Orthopedics INC.
Microport Orthopedics INC. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report