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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Contact Lenses & Vision

MyDay Toric and Other Contact Lenses Recalled for Incorrect Cylinder Power

Agency Publication Date: March 26, 2025
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Summary

CooperVision, Inc. is recalling 33,990 contact lenses, including MyDay Toric and various store brands like Kirkland Signature and LensCrafters, because a limited number of lots were manufactured with the incorrect cylinder power. This defect means the lenses do not match the intended prescription for astigmatism. No injuries or vision-related incidents have been reported to date. Consumers should stop using the affected lenses and contact their eye care professional or the place of purchase for a replacement.

Risk

Wearing contact lenses with the incorrect prescription power can lead to blurred vision, eye strain, and headaches. Inaccurate vision correction can also increase the risk of accidents or injury during activities that require clear sight, such as driving or operating machinery.

What You Should Do

  1. This recall affects various brands of daily disposable contact lenses for astigmatism, including MyDay Toric, LensCrafters One Day Premium, Pearle Vision 1 Day Premium, REVEAL 1-DAY TORIC, Vision Source Reveal Toric, Voyant 1-Day Premium Toric, and Kirkland Signature Toric.
  2. Identify your lenses by checking the lot numbers printed on the individual blister packs or the outer carton. Affected blister lot numbers include 6461501582, 6461501590, 6448502235, and 6472500679. See the Affected Products section below for the full list of affected codes, including carton lot numbers.
  3. Stop using the recalled contact lenses immediately to avoid vision issues.
  4. Return the product to the place of purchase for a refund or replacement, throw it away, or contact your eye care provider or CooperVision, Inc. for further instructions.
  5. If you experience persistent vision problems or eye discomfort after using these products, contact your healthcare provider or eye care professional.
  6. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider, or return the product to the place of purchase for a refund or replacement
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Stop using and throw the product away.

Affected Products

Product: MyDay Toric (Stenfilcon A) Contact Lens
Variants: 54% water content, Toric, Silicone Hydrogel, Daily Disposable
Model / REF:
MyDay Toric
Lot Numbers:
6461501582
6461501590
6448502235
6472500679
19346502595028
344446500117
19346502613
21455502575
21476504025
21545502813
24127502235
40702500019
21512501331
21492501653
21492501685

Includes store brands: LensCrafters One Day Premium, Pearle Vision 1 Day Premium, REVEAL 1-DAY TORIC, Vision Source Reveal Toric, Voyant 1-Day Premium Toric, CADENCE DELUXE 1-DAY TORIC, DUBLAN PREMIUM OXYGEN 1 DAY TORIC, EV LINARIAL TORIC (30), EYEXPERT PURE ASTIGMATISM (30), LENTI!!AS A ASTIGMATISMO 30PK, LENTSOFT DIARIA CONFORT+ SILICONA ASTIGMATISMO, MULTILENS CONTACT ELITE SILICONE 1 DAY TORICS, OPTIONS SUPREME 1 DAY TRC (30), PRIMA + 1 DAY ASTGM (30), PROTECT PLATINUM FOR ASTG (30), SOL- LENS 1 DAY SILICONE PREMIUM TORIC, UGO LENS DAY ADVANCED TORICA, WHITE BOX STENFILCON A TORIC 07536, MEDIFLEX SUP 1D TORIC, Kirkland Signature Toric Premium Daily Disposable, Specsavers easyvision Linarial Toric.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96396
Status: Active
Manufacturer: CooperVision, Inc.
Sold By: LensCrafters; Pearle Vision; Vision Source; Specsavers; Costco; Kirkland Signature
Manufactured In: United States
Units Affected: 33990 lenses (17010 US, 16980 OUS)
Distributed To: California, Colorado, Florida, Illinois, Kentucky, Michigan, North Carolina, Nebraska, New Jersey, New York, Ohio, Oregon, Utah, Virginia, Washington

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.