Drugs & medicalClass II

CooperVision, Inc. recalls MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Silicone Hydrogel,…

One lot manufactured with an invalid sterilization cycle.

Read the official notice →
Date
2025-10-01
Country
United States
Brand
CooperVision
Product
MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Silicone Hydrogel,…
Classification
Class II
Units
US Nationwide distribution in the states of Florida, Kentucky, North Carolina,…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More CooperVision recalls

  1. 2026-09-30
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    CooperVision, Inc. recalls Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day

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    FDA · DeviceCooperVision, Inc.US Nationwide distribution in the states of MN, OH, WI.Official notice →
  3. 2025-07-30
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    CooperVision, Inc. recalls Biofinity XR Toric Contact Lens

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

    FDA · DeviceCooperVision, Inc.Worldwide distribution - US Nationwide and the countries of Brazil, Canada,…Official notice →
  5. 2025-04-02
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    CooperVision, Inc. recalls Brand Names: MyDay Toric, LensCrafters One Day Premium Daily Disposable Contact Lenses For Astigmatism, Pearle Vision 1 Day Premium For…

    a limited number of lots were manufactured with an incorrect cylinder power.

    FDA · DeviceCooperVision, Inc.Domestic: CA, CO, FL, IL, KY, MI, NC, NE, NJ, NY, OH, OR, UT, VA, WA.…Official notice →
  7. 2024-10-09
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    CooperVision, Inc. recalls Biofinity Toric Multifocal Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia with astigmatism)…

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

    FDA · DeviceCooperVision, Inc.Worldwide distribution - US Nationwide and the country of Canada.Official notice →
  9. 2023-03-29
  10. US
    Drugs & medicalClass II

    CooperVision, Inc. recalls Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90

    The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power.

    FDA · DeviceCooperVision, Inc.Worldwide - US Nationwide distribution in the states of FL, IL, NY, UT, and…Official notice →
  11. 2023-03-08
  12. US
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    CooperVision, Inc. recalls Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)

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

    FDA · DeviceCooperVision, Inc.US Nationwide distribution in the states of CA, OH, NC, PA.Official notice →
All 8 CooperVision recalls →

Other drugs & medical recalls in the United States

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    The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa.

    FDA · DeviceBoston Scientific CorporationUS Nationwide distribution in the states of CA, CO, GA, ID, IL, IN, MA, ME,…Official notice →
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    ORTOMA AB recalls Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight REF 30-201 Model Number: 2001 UDI-DI code: 07350137521019 Inserter Adapter OTD…

    Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.

    FDA · DeviceORTOMA ABWorldwide - U.S. Nationwide distribution in the state of FL and the countries…Official notice →
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    The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.

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    Baxter Healthcare Corporation recalls Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8 m),…

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See all drugs & medical recalls →