--- title: "CooperVision, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search CooperVision, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/coopervision-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # CooperVision, Inc. recall records **12** reported ongoing 12 records in this archive. Latest source date Aug 22, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Aug 22, 2025 FDA device enforcement ### [MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily ...](https://isitonrecall.com/recall/fda-device-z-2606-2025-myday-toric-stenfilcon-a-contact-lens-model-catalog-number-myday-toric-54-water-content-toric-cast-m/) One lot manufactured with an invalid sterilization cycle. Class II Reported ongoing Distribution: US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin. [Official source for MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, To...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2606-2025%22) Aug 22, 2025 FDA device enforcement ### [Sofmed Breathables, (stenfilcon A) contact lens. Model Number: Softmed Breathables. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, fo...](https://isitonrecall.com/recall/fda-device-z-2607-2025-sofmed-breathables-stenfilcon-a-contact-lens-model-number-softmed-breathables-54-water-content-toric/) One lot manufactured with an invalid sterilization cycle. Class II Reported ongoing Distribution: US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin. [Official source for Sofmed Breathables, (stenfilcon A) contact lens. Model Number: Softmed Breathables. 54% water con...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2607-2025%22) Aug 22, 2025 FDA device enforcement ### [Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-Day Premium Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, c...](https://isitonrecall.com/recall/fda-device-z-2608-2025-voyant-1-day-premium-toric-stenfilcon-a-contact-lens-model-number-voyant-1-day-premium-toric-54-wate/) One lot manufactured with an invalid sterilization cycle. Class II Reported ongoing Distribution: US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin. [Official source for Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-Day Premium Toric...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2608-2025%22) Jun 16, 2025 FDA device enforcement ### [Biofinity XR Toric Contact Lens](https://isitonrecall.com/recall/fda-device-z-2165-2025-biofinity-xr-toric-contact-lens/) Lens blisters may have an incomplete or leaking seal which may render them unsterile. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Brazil, Canada, Honduras, and Mexico. [Official source for Biofinity XR Toric Contact Lens](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2165-2025%22) Jun 16, 2025 FDA device enforcement ### [Biofinity Toric Multifocal Contact Lens](https://isitonrecall.com/recall/fda-device-z-2166-2025-biofinity-toric-multifocal-contact-lens/) Lens blisters may have an incomplete or leaking seal which may render them unsterile. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Brazil, Canada, Honduras, and Mexico. [Official source for Biofinity Toric Multifocal Contact Lens](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2166-2025%22) Feb 27, 2025 FDA device enforcement ### [Brand Names: MyDay Toric, LensCrafters One Day Premium Daily Disposable Contact Lenses For Astigmatism, Pearle Vision 1 Day Premium For Astigmatism, REVEAL 1-DAY TORIC, Vision S...](https://isitonrecall.com/recall/fda-device-z-1455-2025-brand-names-myday-toric-lenscrafters-one-day-premium-daily-disposable-contact-lenses-for-astigmatism/) a limited number of lots were manufactured with an incorrect cylinder power. Class II Reported ongoing 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, Luxemb... [Official source for Brand Names: MyDay Toric, LensCrafters One Day Premium Daily Disposable Contact Lenses For Astigm...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1455-2025%22) Aug 29, 2024 FDA device enforcement ### [BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia with astigmatism) with presbyopia in aphakic and non-aphakic persons.](https://isitonrecall.com/recall/fda-device-z-3310-2024-biofinity-xr-toric-lenses-soft-contact-lenses-indicated-for-the-correction-of-ametropia-myopia-or-hy/) Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Canada. [Official source for BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3310-2024%22) Aug 29, 2024 FDA device enforcement ### [Biofinity Toric Multifocal Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia with astigmatism) with presbyopia in aphakic and non-aphak...](https://isitonrecall.com/recall/fda-device-z-3311-2024-biofinity-toric-multifocal-lenses-soft-contact-lenses-indicated-for-the-correction-of-ametropia-myop/) Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Canada. [Official source for Biofinity Toric Multifocal Lenses - Soft Contact lenses Indicated for the correction of ametropia...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3311-2024%22) Feb 14, 2023 FDA device enforcement ### [Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90](https://isitonrecall.com/recall/fda-device-z-1282-2023-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. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of FL, IL, NY, UT, and WI. The country of Canada. [Official source for Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1282-2023%22) Jan 26, 2023 FDA device enforcement ### [Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)](https://isitonrecall.com/recall/fda-device-z-1197-2023-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 Class II Reported ongoing Distribution: US Nationwide distribution in the states of CA, OH, NC, PA. [Official source for Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1197-2023%22) Jan 26, 2023 FDA device enforcement ### [Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens (extended wear)](https://isitonrecall.com/recall/fda-device-z-1198-2023-biofinity-xr-toric-single-diagnostic-lens-soft-hydrophilic-contact-lens-extended-wear/) Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity Class II Reported ongoing Distribution: US Nationwide distribution in the states of CA, OH, NC, PA. [Official source for Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens (extended wear)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1198-2023%22) Dec 27, 2022 FDA device enforcement ### [MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). Single Use.](https://isitonrecall.com/recall/fda-device-z-1014-2023-myday-toric-90-pack-reveal-1-day-toric-90-pack-soft-hydrophilic-contact-lens-daily-wear-single-use/) Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity. Class II Reported ongoing Distribution: Distribution to US states of CA, FL, IA, KY, NC, NY, OH, OR, WI; Canada and Japan. [Official source for MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1014-2023%22) ## Reasons in these listed records - One lot manufactured with an invalid sterilization cycle. - Lens blisters may have an incomplete or leaking seal which may render them unsterile. - a limited number of lots were manufactured with an incorrect cylinder power. - Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity These examples come from this result page and are not a ranking of every recall reason. ## Checking CooperVision, Inc. ### Is there a recall on coopervision, inc. right now? This archive contains 12 records, including 12 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search CooperVision, Inc.](https://isitonrecall.com/check/?q=CooperVision%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)