Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY Recalled by MicroPort Orthopedics Inc. Due to Femoral implant porous size 5 right primary and...
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 FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR NON-POROUS SIZE 6 LEFT PRIMARY, REF: EFSRN6PL Knee prosthesis component
Quantity: 32
Why Was This Recalled?
Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packaging.
Where Was This Sold?
OUS: CN, GR, ES, ZA, FR, JP, IT
About MicroPort Orthopedics Inc.
MicroPort Orthopedics Inc. has 30 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report