Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
NeuraGen Nerve Guide Recalled by Integra LifeSciences Corp. Due to Nonconforming product which was dispositioned for rejection was...
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
NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated for the repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.
Quantity: 55
Why Was This Recalled?
Nonconforming product which was dispositioned for rejection was mistakenly released for commercial use.
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