CooperVision, Inc. MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). Single Use. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). Single Use.
Brand
CooperVision, Inc.
Lot Codes / Batch Numbers
Lot 6474502034 - packaged into 2 packaging lots: 21514501939036, 21514501972036 No UDI
Products Sold
Lot 6474502034 - packaged into 2 packaging lots: 21514501939036, 21514501972036 No UDI
CooperVision, Inc. is recalling MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). Si due to Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity.
Recommended Action
Per FDA guidance
On December 27, 2022, the firm notified affected wholesale/distributor and Eye Care Practitioner consignees via Urgent Medical Device Correction letters. Customers were instructed to stop any further distribution of product from affected lot numbers and dispose of any affected product still in inventory. Customers may also return product. Customers who are affected by this recall are eligible for credit or replacement. Distributors and Eye Care Practitioners should also contact downstream Eye Care Practitioner customers as well as patients who have received product from the affected lots. Patients with questions may contact CooperVision's Customer Service team at 800-341-2020, 9:00 AM 7:00 PM ET, Monday Friday, or they can visit CooperVision s website at coopervision.com/our-company/contact-us/complaint.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, FL, IA, KY, NY, NC, OH, OR, WI
Page updated: Jan 10, 2026