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Lower risk Medical device recall · FDA · Published May 19, 2021

CooperVision SPECSAVERS UMERE TORIC Contact Lens Recall: Blurred Vision Risk

CooperVision recalls SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lenses with UV blocker due to potential blurred vision from misaligned axis marks. Affected lenses have Lot Number U0108940.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2148-2021Medical deviceCooperVision ›
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Contact the company

Recalling firmCooperVision Inc.180 Thruway Park Dr · West Henrietta, NY 14586-9798
✎ GovInfoNow plain-language explainer

CooperVision is recalling a specific type of daily disposable contact lens that may cause blurred vision if the axis mark is misaligned. This issue could affect users who rely on precise lens alignment for clear vision. Read more at govinfonow.com/recall/62506-coopervision-specsavers-umere-toric-contact-lens-recall-blurred-vision-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/62506-coopervision-specsavers-umere-toric-contact-lens-recall-blurred-vision-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2148-2021

Cite this page

“CooperVision SPECSAVERS UMERE TORIC Contact Lens Recall: Blurred Vision Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62506-coopervision-specsavers-umere-toric-contact-lens-recall-blurred-vision-risk. Based on FDA recall #Z-2148-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2148-2021%22&limit=1).

CooperVision Inc. recalled SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lenses with UV blocker due to a misaligned axis mark that can cause blurred vision, the FDA said on May 19, 2021.

How to tell if you have it

  • Brand: CooperVision
  • Product: SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
  • Lot Number: U0108940
  • Quantity: 60 lenses

The hazard

The recall addresses the misaligned placement of an axis mark on the contact lenses, which can cause patients to experience blurred vision.

Context

GovInfoNow's records show CooperVision, Inc. has had 11 other recalls since September 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 TECNIS Eyhance IOL with Simplicity Delivery System Recall (February 19, 2026).

How to tell if you have this one

Check for the product name 'SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker' and Lot Number U0108940 on the packaging or lens box.

  • Brand
    CooperVision
  • Category
    Medical device
FDA recall event · 12 products

All 12 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Worldwide distribution - US Nationwide distribution in the states of FL, NY, TN, OH, NC, WI and the countries of France, United Arab Emirates, Brazil, Australia, New Zealand, Taiwan, Canada.
Recall numberProduct, codes & lotsQuantity
Z-2143-2021CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker; Lot Number: R012162990 lenses
Z-2144-2021AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker; Lot Number: R0121629720 lenses
Z-2145-2021FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker; Lot Number: R012162990 lenses
Z-2146-2021CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker; Lot Number: U010883390 lenses
Z-2147-2021CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker; Lot Number: U01089401260 lenses
Z-2148-2021SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker; Lot Number: U010894060 lenses
Z-2149-2021CLARITI 1 DAY TORIC -DIAGNOSTIC Power-07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker; Lot Number: W010616710 lenses
Z-2150-2021CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker; Lot Number: W0106167450 lenses
Z-2151-2021MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker; Lot Number: W010616790 lenses
Z-2152-2021CLARITI 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker; Lot Number: W0106186450 lenses
Z-2153-2021FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker; Lot Number: W0106186180 lenses
Z-2154-2021SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 Daily Disposable Contact Lens with UV blocker; Lot Number: W010616790 lenses
Based on the official FDA remedy

What to do — step by step

  1. Check Lens Packaging

    Look for the Lot Number U0108940 on the lens packaging or box to confirm if it's affected.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 6 states.

Alaska: nationwideAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: nationwideWAIdaho: nationwideIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: nationwideILWisconsin: named in the noticeWIMichigan: nationwideMINew York: named in the noticeNYRhode Island: nationwideRIMassachusetts: nationwideMAOregon: nationwideORNevada: nationwideNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: nationwideIAIndiana: nationwideINOhio: named in the noticeOHPennsylvania: nationwidePANew Jersey: nationwideNJConnecticut: nationwideCTCalifornia: nationwideCAUtah: nationwideUTColorado: nationwideCONebraska: nationwideNEMissouri: nationwideMOKentucky: nationwideKYWest Virginia: nationwideWVVirginia: nationwideVAMaryland: nationwideMDDelaware: nationwideDEArizona: nationwideAZNew Mexico: nationwideNMKansas: nationwideKSArkansas: nationwideARTennessee: named in the noticeTNNorth Carolina: named in the noticeNCSouth Carolina: nationwideSCDistrict of Columbia: nationwideDCOklahoma: nationwideOKLouisiana: nationwideLAMississippi: nationwideMSAlabama: nationwideALGeorgia: nationwideGAHawaii: nationwideHITexas: nationwideTXFlorida: named in the noticeFL

FDA distribution: “Worldwide distribution - US Nationwide distribution in the states of FL, NY, TN, OH, NC, WI and the countries of France, United Arab Emirates, Brazil, Australia, New Zealand, Taiwan, Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Florida, New York, North Carolina, Ohio, Tennessee, Wisconsin.

Recall timeline

FDA terminated this recall 22 months after the firm started it.

1. Firm started the recall: May 19, 202112. FDA classified it Class II: Jul 27, 202123. Published in FDA’s Enforcement Report: Aug 4, 202134. FDA terminated the recall: Mar 13, 2023420212023
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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-2148-2021 (May 19, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2148-2021 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA