CooperVision Recalls Clariti 1 Day Contact Lenses for Incorrect Expiration Date
CooperVision is recalling Clariti 1 Day contact lenses because the secondary packaging displays an incorrect expiration date.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class III, which by definition is unlikely to cause adverse health consequences. The issue is a packaging labeling error regarding the expiration date, which falls under the 'Low' severity criteria for documentation or packaging-only problems.
Plain-English summary
CooperVision Inc. is recalling Clariti 1 Day (-1.25) 90 pack, UV Blocking, silicone hydrogel, daily disposable contact lenses. The recall is due to the secondary packaging being labeled with an incorrect expiration date.
The affected product is Lot 14377101733005, with an expiration date of 6/30/2020 on the foil and 6/20/2030 on the carton. The quantity involved is 32 packs, containing 2,880 lenses. The product was distributed nationwide to specific states including AL, AR, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NY, OH, OR, PA, SC, TN, TX, UT, VA, WA, WI, and WY.
Consumers with this product should stop using it and contact CooperVision Inc. for further instructions.
The recalled product
- Product
- clariti 1 day (-1.25) 90 pack, UV Blocking, 90 silicone hydrogel, daily disposable contact lenses The Clariti 1 Day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV blocker is indicated for daily wear single use only for the correction of refractiveamet
- Manufacturer
- CooperVision Inc.
- Category
- Medical Device — Contact Lenses
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Lot 14377101733005
- Exp. Date 6/30/2020 (foil)
- 6/20/2030 (carton)
Distribution
Part of a larger recall action
This product is one of 4 recalled by CooperVision Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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