Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Nextra Hammertoe Correction System-4.5MM Middle Recalled by Nextremity Solutions Due to Proximal end of the driver in the affected...
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 Nextremity Solutions directly.
Affected Products
Nextra Hammertoe Correction System-4.5MM Middle, 3.2MM Proximal, SS, Sterile. REF: NX-4532K - Product Usage: The Nextra Hammertoe Correction System is a system of implants and associated instruments which is indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes.
Quantity: 190 units
Why Was This Recalled?
Proximal end of the driver in the affected product may be oversized in varying degrees, potentially making it difficult to connect with and remove from the proximal Nextra implant
Where Was This Sold?
International distribution in the countries of Spain, United Kingdom, Germany, and Switzerland.
About Nextremity Solutions
Nextremity Solutions has 15 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report