Reported Oct 9, 2024 · Ongoing

Biofinity Toric Multifocal Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia…

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 Toric Multifocal 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

    584 of 584 codes

    • RB0444532
    • RB0450357
    • RB0450370
    • RB0450372
    • RB0450378
    • RB0450379
    • RB0450407
    • RB0450419
    • RB0450422
    • RB0450429
    • RB0450438
    • RB0450446
    • RB0450455
    • RB0450457
    • RB0450465
    • RB0450466
    • RB0450477
    • RB0450478
    • RB0450496
    • RB0450501
    • RB0450504
    • RB0450542
    • RB0450547
    • RB0450548
    • RB0450560
    • RB0450561
    • RB0450575
    • RB0450594
    • RB0450613
    • RB0450625
    • RB0450636
    • RB0450646
    • RB0450649
    • RB0450653
    • RB0450657
    • RB0450659
    • RB0450686
    • RB0450687
    • RB0450688
    • RB0450691
    • RB0450693
    • RB0450694
    • RB0450695
    • RB0450697
    • RB0450699
    • RB0450701
    • RB0450702
    • RB0450707
    • RB0450708
    • RB0450709
    • RB0450710
    • RB0450714
    • RB0450719
    • RB0450727
    • RB0450730
    • RB0450739
    • RB0450746
    • RB0450748
    • RB0450753
    • RB0450767
Amount recalled
2443 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, 6:57 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.