Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Integra PANTA Arthrodesis Nail System. Intended for use in tibiotalocalcaneal Recalled by Integra LifeSciences Corporation Due to As a result of the investigation into an...
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 Corporation directly.
Affected Products
Integra PANTA Arthrodesis Nail System. Intended for use in tibiotalocalcaneal arthrodesis and treatment of trauma to the hindfoot and distal tibia.
Quantity: 692
Why Was This Recalled?
As a result of the investigation into an adverse trend of complaints for reports of misalignment of the calcaneal or tibial screws during use of the Panta Nail Support Device, Integra has decided to issue this voluntary medical device correction. The misalignment can result in the inability to properly insert the screws into the Panta Nail and create the potential need for revision surgery.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Integra LifeSciences Corporation
Integra LifeSciences Corporation has 29 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report