Reported Jul 30, 2025 · Ongoing

Biofinity XR Toric Contact Lens

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. · 711 North Rd · Scottsville, NY · 14546-1238

Is this the product you have?

  • Biofinity XR Toric Contact Lens
Lot codes and dates
  • Carton Lot Numbers

    78 of 78 codes

    • RD0226792
    • RD0227007
    • RD0227022
    • RD0227030
    • RD0227032
    • RD0228123
    • RD0228336
    • RD0228465
    • RD0228570
    • RD0228595
    • RD0228598
    • RD0228603
    • RD0228606
    • RD0228607
    • RD0228775
    • RD0228778
    • RD0228788
    • RD0228795
    • RD0228798
    • RD0228799
    • RD0228802
    • RD0228809
    • RD0228814
    • RD0228825
    • RD0228835
    • RD0228840
    • RD0228842
    • RD0228847
    • RD0228853
    • RD0228854
    • RD0228855
    • RD0228866
    • RD0228875
    • RD0228876
    • RD0228940
    • RE0152731
    • RE0152735
    • RE0152737
    • RE0152740
    • RE0152743
    • RE0152744
    • RE0152755
    • RE0152760
    • RE0152775
    • RE0152799
    • RE0152838
    • RE0152871
    • RE0152873
    • RE0152877
    • RE0152883
    • RE0152889
    • RE0152891
    • RE0152913
    • RE0152915
    • RE0152917
    • RE0153804
    • RE0153819
    • RE0153924
    • RE0153974
    • RE0154076
Amount recalled
397 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Lens blisters may have an incomplete or leaking seal which may render them unsterile.

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 Sep 19, 5:39 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.