CooperVision, Inc. is recalling 33,990 contact lenses, including MyDay Toric and various store brands like Kirkland Signature and LensCrafters, because a limited number of lots were manufactured with the incorrect cylinder power. This defect means the lenses do not match the intended prescription for astigmatism. No injuries or vision-related incidents have been reported to date. Consumers should stop using the affected lenses and contact their eye care professional or the place of purchase for a replacement.
Wearing contact lenses with the incorrect prescription power can lead to blurred vision, eye strain, and headaches. Inaccurate vision correction can also increase the risk of accidents or injury during activities that require clear sight, such as driving or operating machinery.
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Includes store brands: LensCrafters One Day Premium, Pearle Vision 1 Day Premium, REVEAL 1-DAY TORIC, Vision Source Reveal Toric, Voyant 1-Day Premium Toric, CADENCE DELUXE 1-DAY TORIC, DUBLAN PREMIUM OXYGEN 1 DAY TORIC, EV LINARIAL TORIC (30), EYEXPERT PURE ASTIGMATISM (30), LENTI!!AS A ASTIGMATISMO 30PK, LENTSOFT DIARIA CONFORT+ SILICONA ASTIGMATISMO, MULTILENS CONTACT ELITE SILICONE 1 DAY TORICS, OPTIONS SUPREME 1 DAY TRC (30), PRIMA + 1 DAY ASTGM (30), PROTECT PLATINUM FOR ASTG (30), SOL- LENS 1 DAY SILICONE PREMIUM TORIC, UGO LENS DAY ADVANCED TORICA, WHITE BOX STENFILCON A TORIC 07536, MEDIFLEX SUP 1D TORIC, Kirkland Signature Toric Premium Daily Disposable, Specsavers easyvision Linarial Toric.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES ยท Raw API Response
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