Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CryoTreQ- Aa disposable handheld instrument intended for ophthalmic surgery. It Recalled by Beaver Visitec International, Inc. Due to Device suddenly and forcefully disassembled after cryotherapy, potential...
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 Beaver Visitec International, Inc. directly.
Affected Products
CryoTreQ- Aa disposable handheld instrument intended for ophthalmic surgery. It creates a tip at cryogenic temperatures by evaporation of N2O that can be utilized to perform cryotherapy based on the destruction of tissue by extreme cold to locally perform cryocoagulation on tissue. Ref: CT00.D01
Quantity: 501 (USA)
Why Was This Recalled?
Device suddenly and forcefully disassembled after cryotherapy, potential for long-term or permanent impairment of a patient or user if a CryoTreq device suddenly or forcefully disassembles during a cryosurgery procedure.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Beaver Visitec International, Inc.
Beaver Visitec International, Inc. has 180 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report