Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Integra Cadence Total Ankle System Recalled by Integra LifeSciences Corp. Due to Posterior tibial fractures have been reported.
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 Integra LifeSciences Corp. directly.
Affected Products
Integra Cadence Total Ankle System
Quantity: 944 units
Why Was This Recalled?
Posterior tibial fractures have been reported.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Integra LifeSciences Corp.
Integra LifeSciences Corp. has 216 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report