CooperVision, Inc. recalls MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Numbe
See all recalls from CooperVision, Inc. →Recalled Product
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 Disposable Wear. Blister packaged.
Hazard / Issue
One lot manufactured with an invalid sterilization cycle.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for MyDay Toric, stenfilcon A) →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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