Reported Oct 28, 2026 · Ongoing · Updated Nov 2, 2026

Generic Name: Softmed Breathables Advanced Toric (fanfilcon A) Soft (Hydrophilic) Contact Lens; Model/Catalog Number:…

CooperVision, Inc.

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: CooperVision, Inc. · 180 Thruway Park Dr · West Henrietta, NY · 14586-9798

Is this the product you have?

  • Generic NameSoftmed Breathables Advanced Toric (fanfilcon A) Soft (Hydrophilic) Contact Lens
  • Model/Catalog NumberSoftmed Breathables
  • Advanced Toric Product Description55% water content, toric, silicone hydrogel contact lens for daily wear, frequent replacement. Blister packaged
Lot codes and dates
  • Model/Catalog NumberSoftmed Breathables Advanced Toric
  • UDI-DIN/A
  • Lot numbers

    2,033 of 2,033 codes

    • 19486120027517
    • 19486120030515
    • 19486120035532
    • 19486120051506
    • 19486170015507
    • 19486170016513
    • 19486170016521
    • 19486170017507
    • 19486170017509
    • 19486170017512
    • 19486170019512
    • 19486170019514
    • 19486170021021
    • 19486170021518
    • 19486170022503
    • 19486170022504
    • 19486170023528
    • 19486170025508
    • 19486170026021
    • 19486170027034
    • 19486170027504
    • 19486170027524
    • 19486170028518
    • 19486170030023
    • 19486170030034
    • 19486170031023
    • 19486170031034
    • 19486170032030
    • 19486170032036
    • 19486170032504
    • 19486170033501
    • 19486170034001
    • 19486170034032
    • 19486170034038
    • 19486170039040
    • 19486170040030
    • 19486170041032
    • 19486170042018
    • 19486170042032
    • 19486170043003
    • 19486170043028
    • 19486170043030
    • 19486170043032
    • 19486170043502
    • 19486170044017
    • 19486170045011
    • 19486170047002
    • 19486170047007
    • 19486170047011
    • 19486170048011
    • 19486170049004
    • 19486170049006
    • 19486170049009
    • 19486170049011
    • 19486170050003
    • 19486170050004
    • 19486170050007
    • 19486170050019
    • 19486170051002
    • 19486170051006
Amount recalled
230856

Where it was sold

Why it was recalled

The affected products bear an incorrect statement on the carton packaging indicating that the product is "Indicated for Extended Wear". However, this product is intended for daily wear, and the extended-wear statement should not have appeared on the affected carton labeling. This product is not approved by the U.S. Food and Drug Administration (FDA) for extended wear use.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 12:11 AM 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.