Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AURORA Surgiscope System Recalled by Integra LifeSciences Corp. Due to Possibility for the obturator to break (separate).
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
AURORA Surgiscope System, Sterile, single use device that contains a Sheath, Obturator, and Imager. Manufacturer's Product Numbers (Catalog Number): (1) ASX15/60 and (2) ASX15/80
Quantity: 623 units
Why Was This Recalled?
Possibility for the obturator to break (separate).
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