Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A) Recalled by Bausch & Lomb Inc Irb Due to The firm determined that 25 lots had been...
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 Bausch & Lomb Inc Irb directly.
Affected Products
BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A), Product Order Number Biotrue SVS - 7201, STERILE, Rx Only; The lenses are available in 5 pack, 30 pack and 90 pack sizes; Biotrue ONEday Foil - Part Number 8098001, Biotrue ONEday 5 pack Carton International - Part Number 8101403, and Biotrue ONEday 90 pack Carton International - Part Number 8098203.
Quantity: Domestic: 99,260 lenses; Foreign: 84,660 lenses
Why Was This Recalled?
The firm determined that 25 lots had been manufactured with a minor surface defect occurring in the optical surface on each lens. Complaints of Halo or Poor Visual Acuity.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bausch & Lomb Inc Irb
Bausch & Lomb Inc Irb has 48 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report