Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PROFEMUR(R) MODULAR NECK Recalled by MicroPort Orthopedics Inc. Due to Profemur(R) neck, Item Number PHA01222 (Short AR VV2...
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
PROFEMUR(R) MODULAR NECK, HIP FEMORAL NECK MicroPort total hip systems intended for use in total hip arthroplasty for reduction or relief of pain and/or improved hip function in skeletally mature patients.
Quantity: 14 units
Why Was This Recalled?
Profemur(R) neck, Item Number PHA01222 (Short AR VV2 Ti Neck) was labeled as Item Number PHA01212 (Short AR VV1 Ti Neck).
Where Was This Sold?
Belgium, Italy, Spain, and Poland
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