Reported Nov 11, 2015 · Terminated

BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A), Product Order Number Biotrue SVS - 7201, STERILE, Rx Only; The…

Bausch & Lomb Inc. Irb

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Bausch & Lomb Inc Irb · 1400 Goodman St N · Rochester, NY · 14609-3547

Is this the product you have?

  • 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.
Lot codes and dates
  • Select -2.25/-3.00
  • Diopter Lot Numbers
    • W57209820 (exp. date 05/19/2019)
    • W57210174 (exp. date 05/23/2019)
    • W57210440 (exp. date 05/28/2019)
    • W57211652 (exp. date 06/09/2019)
    • W57211916 (exp. date 06/09/2019)
    • W57212210 (exp. date 06/09/2019)
    • W57212440 (exp. date 06/09/2019)
    • W57212697 (exp. date 06/09/2019)
    • W57212926 (exp. date 06/09/2019)
    • W57213158 (exp. date 06/09/2019)
    • W57213453 (exp. date 06/09/2019)
    • W57213743 (exp. date 07/01/2019)
    • W57213969 (exp. date 07/01/2019)
    • W57214208 (exp. date 07/01/2019)
    • W57214459 (exp. date 07/01/2019)
    • W57214717 (exp. date 07/01/2019)
    • W57215039 (exp. date 07/01/2019)
    • W57215293 (exp. date 07/01/2019)
    • W57215517 (exp. date 07/01/2019)
    • W57215783 (exp. date 07/01/2019)
Amount recalled
Domestic: 99,260 lenses; Foreign: 84,660 lenses

Where it was sold

  • Nationwide

Why it was 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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 6, 2016 · Data as of Sep 19, 4:44 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.