Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120. Product Description: Recalled by Iantrek Inc. Due to Potential for compromised integrity of the sterile packaging.
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 Iantrek Inc. directly.
Affected Products
C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120. Product Description: The C-Rex UNO Microinterventional Goniotomy Instrument is a sterile single use disposable manual surgical instrument used in ophthalmic procedures for ab interno goniotomy and inner wall trabeculotomy.
Quantity: 198
Why Was This Recalled?
Potential for compromised integrity of the sterile packaging.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Iantrek Inc.
Iantrek Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report