Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Recalled by Integra LifeSciences Corp. Due to Potential for certain SKUs and lot numbers were...
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
CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810 Implantable device that provides constant intraventricular pressure and drainage of CSF for the management of hydrocephalus.
Quantity: 132 units
Why Was This Recalled?
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
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