“CooperVision Clariti 1-day toric lenses recalled for incorrect power.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/58898-coopervision-clariti-1-day-toric-lenses-recalled-for-incorrect-power. Based on FDA recall #Z-1282-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1282-2023%22&limit=1).
CooperVision, Inc. voluntarily recalled Clariti 1-day toric soft contact lenses on Feb. 14, 2023, after the FDA announced the product had incorrect power due to a misaligned axis. The recall affects 3,150 units distributed in Florida, Illinois, New York, Utah, Wisconsin and Canada.
How to tell if you have it
Brand: CooperVision
Product: Clariti 1-day toric soft contact lenses
Power: -1.00 -1.25/90
Lot Number: W0124677
The hazard
The lenses were manufactured with a misaligned axis, resulting in incorrect power for the wearer. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show CooperVision has 11 other recalls on record since Sept. 1, 2017. Other recent recalls include CooperVision Pearle Vision 1 Day Contact Lenses (Aug. 12, 2026), CooperVision MyDay Toric Contact Lenses (Aug. 22, 2025) and CooperVision Biofinity XR Toric Contact Lenses (June 16, 2025).
How to tell if you have this one
Check if your lenses have the lot number W0124677. The product is Clariti 1-day toric soft contact lenses with power -1.00 -1.25/90.
Brand
CooperVision
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Lens Lot Number
Look for the lot number W0124677 on your lens packaging or container.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 5 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide - US Nationwide distribution in the states of FL, IL, NY, UT, and WI. The country of Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Florida, Illinois, New York, Utah, Wisconsin.
Recall timeline
FDA published this recall 43 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-1282-2023 (February 14, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1282-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.