Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone Recalled by Nextremity Solutions Due to During insertion of the middle phalanx implant into...
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 CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes SKU: CH-MINI-KT
Quantity: 23 units
Why Was This Recalled?
During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx implants, resulting in surgical delay, in-situ removal of the implant, use of alternative surgical approach, disassembly of the implants post-operatively, and revision
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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