Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Integra Straight Ventricular Catheter F8 Recalled by Integra LifeSciences Corp. Due to During final sampling inspection, one of the lots...
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 Straight Ventricular Catheter F8, 25 cm, Sterile EO, Rx only, packaged in a Tyvek pouch and secondary packaged in to Tyvek pouch, sealed in a cardboard box. Silicone elastomer Ventricular Catheter for use with hydrocephalus valves
Quantity: 10
Why Was This Recalled?
During final sampling inspection, one of the lots was discovered with a total incomplete packaging seal of the sterile product.
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