Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Recalled by Beaver-Visitec International Inc. Due to Devon Light Glove in procedure kits may have...
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
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584569 Ophthalmic surgical kits
Quantity: 621 kits
Why Was This Recalled?
Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Beaver-Visitec International Inc.
Beaver-Visitec International Inc. has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report