CooperVision MyDay Toric Contact Lenses Recall: Incorrect Cylinder Power
CooperVision recalls limited lots of MyDay Toric contact lenses for astigmatism due to incorrect cylinder power. Consumers should check lot numbers and contact CooperVision for a replacement.
Lower-risk recall
a limited number of lots were manufactured with an incorrect cylinder power.
Contact the company
What happened, in plain English
CooperVision is recalling specific lots of MyDay Toric contact lenses for astigmatism because some were made with the wrong cylinder power. This could lead to improper vision correction and discomfort or eye damage if worn. Read more at govinfonow.com/recall/52737-coopervision-myday-toric-contact-lenses-recall-incorrect-cylinder-power.
Source Summary by GovInfoNow · govinfonow.com/recall/52737-coopervision-myday-toric-contact-lenses-recall-incorrect-cylinder-power · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1455-2025
Cite this page
“CooperVision MyDay Toric Contact Lenses Recall: Incorrect Cylinder Power.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52737-coopervision-myday-toric-contact-lenses-recall-incorrect-cylinder-power. Based on FDA recall #Z-1455-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1455-2025%22&limit=1).
Why it’s dangerous
The lenses were manufactured with an incorrect cylinder power, which means they may not correct astigmatism properly. This can cause blurred vision, eye strain, or discomfort when worn.
Who’s affected
Contact lens wearers who purchased the recalled MyDay Toric, LensCrafters One Day Premium Daily Disposable, or similar brands with the listed lot numbers are affected. People with astigmatism who use these lenses daily are most at risk.
How to tell if you have this one
Check the blister pack lot numbers: 6461501582, 6461501590, 6448502235, or 6472500679. Also look for carton lot numbers listed in the record.
- Brand
CooperVision- Category
Medical device
What to do — step by step
Check Lot Numbers
Look for blister pack lot numbers: 6461501582, 6461501590, 6448502235, or 6472500679.
Contact CooperVision
Reach out to CooperVision for a replacement or refund if you have the recalled lot numbers.
Where it went and when
Where it was distributed
Distributed in 15 states, and outside the U.S.
FDA distribution: “Domestic: CA, CO, FL, IL, KY, MI, NC, NE, NJ, NY, OH, OR, UT, VA, WA. International: Australia, Belgium, Canada, Czech Republic, Denmark, France, Germany, Ireland, Italy, Luxembourg, Netherlands, New Zealand, Norway, Poland, Portugal,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Colorado, Florida, Illinois, Kentucky, Michigan, Nebraska, New Jersey, New York, North Carolina, Ohio, Oregon, Utah, Virginia, Washington.
Recall timeline
FDA published this recall 34 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1455-2025 (February 27, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1455-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.