Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM Recalled by Medacta Usa Inc Due to Complaint monitoring noted a trend of packaging being...
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 Medacta Usa Inc directly.
Affected Products
Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless use in total or partial hip arthroplasty in primary or revision surgery.
Quantity: 837 units
Why Was This Recalled?
Complaint monitoring noted a trend of packaging being breached for the MiniMAX Stem.
Where Was This Sold?
This product was distributed to 2 states: ID, NC
About Medacta Usa Inc
Medacta Usa Inc has 16 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report