Reported Oct 9, 2024 · Ongoing

BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia with…

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?

  • BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia with astigmatism) with presbyopia in aphakic and non-aphakic persons.
Lot codes and dates
  • UDI-DIN/A
  • Lot Numbers

    134 of 134 codes

    • RD0122830
    • RD0122954
    • RD0122963
    • RD0123016
    • RD0123055
    • RD0123135
    • RD0123147
    • RD0123159
    • RD0123160
    • RD0123172
    • RD0123187
    • RD0123193
    • RD0123197
    • RD0123206
    • RD0123212
    • RD0123250
    • RD0123254
    • RD0123261
    • RD0123265
    • RD0123268
    • RD0123284
    • RD0123294
    • RD0123307
    • RD0123321
    • RD0123323
    • RD0123327
    • RD0123346
    • RD0123347
    • RD0123379
    • RD0123382
    • RD0123404
    • RD0123405
    • RD0123408
    • RD0123419
    • RD0123428
    • RD0123433
    • RD0123442
    • RD0123488
    • RD0123492
    • RD0123499
    • RD0123507
    • RD0123535
    • RD0123551
    • RD0123587
    • RD0123595
    • RD0123610
    • RD0123615
    • RD0123619
    • RD0123628
    • RD0123646
    • RD0123657
    • RD0123667
    • RD0123675
    • RD0123698
    • RD0123701
    • RD0123705
    • RD0123728
    • RD0123730
    • RD0123734
    • RD0123751
Amount recalled
607 lenses

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

Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity

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, 6:19 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.