Lower riskMedical device recall · FDA · Published December 27, 2022
CooperVision MyDay Toric Contact Lenses Recall: Incorrect Power Risk
CooperVision recalls 90-pack MyDay Toric and Reveal : Lenses may have incorrect power causing poor vision. Affected customers should contact for remedy.
“CooperVision MyDay Toric Contact Lenses Recall: Incorrect Power Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59052-coopervision-myday-toric-contact-lenses-recall-incorrect-power-risk. Based on FDA recall #Z-1014-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1014-2023%22&limit=1).
The FDA announced on December 27, 2022, that CooperVision, Inc. is recalling MyDay Toric and Reveal 1 Day Toric soft contact lenses due to a potential incorrect power hazard. Owners should stop using the affected lenses immediately.
How to tell if you have it
Brand: CooperVision
Products: MyDay Toric (90-pack), Reveal 1 Day Toric (90-pack)
Lot code: 6474502034
Packaging lots: 21514501939036, 21514501972036
Units affected: 6,570 lenses
The hazard
The lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity.
Context
GovInfoNow's records show CooperVision, Inc. has 11 other recalls on record since September 1, 2017. Other recent recalls include CooperVision Pearle Vision 1 Day Contact Lenses (August 12, 2026), CooperVision MyDay Toric Contact Lenses (August 22, 2025), and CooperVision Biofinity XR Toric Contact Lenses (June 16, 2025). Other recent recalls of similar products include Olympus 4K UHD Monitor Recall (July 7, 2026).
How to tell if you have this one
Check for the product names 'MyDay Toric (90-pack)' or 'Reveal 1 Day Toric (90-pack)' and lot numbers 21514501939036 or 21514501972036. The lenses have no UDI (Unique Device Identification).
Brand
CooperVision
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Contact CooperVision
Reach out to CooperVision for assistance with the recall.
Where it went and when
Where it was distributed
Distributed in 9 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “Distribution to US states of CA, FL, IA, KY, NC, NY, OH, OR, WI; Canada and Japan.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Florida, Iowa, Kentucky, New York, North Carolina, Ohio, Oregon, Wisconsin.
Recall timeline
FDA published this recall 36 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-1014-2023 (December 27, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1014-2023 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.