Clerio Vision EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for daily wear - Product Usage: indicated for the correction of visual acuity in aphakic or not-aphakic persons with non-diseased eyes that are myopic or hyperopic. The lens may be worn by persons who exhibit astigmatism of 0.75 Diopters or less that does not interfere with visual acuity. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for daily wear - Product Usage: indicated for the correction of visual acuity in aphakic or not-aphakic persons with non-diseased eyes that are myopic or hyperopic. The lens may be worn by persons who exhibit astigmatism of 0.75 Diopters or less that does not interfere with visual acuity.
Brand
Clerio Vision
Lot Codes / Batch Numbers
Lot Number: 0114511565, UPC Code: 675506700657 (6 pack), 675506668650 (individual)
Products Sold
Lot Number: 0114511565, UPC Code: 675506700657 (6 pack), 675506668650 (individual)
Clerio Vision is recalling EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for daily wear - Product Usage: indicate due to Contact lenses may be mislabeled with the incorrect lens power.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Contact lenses may be mislabeled with the incorrect lens power.
Recommended Action
Per FDA guidance
Customers were contacted by phone on 02/16/2021 and instructed to segregate and return product with the affected lot number. An URGENT MEDICAL DEVICE RECALL were sent to impacted customers by standard USPS first class mail beginning on 03/03/2021. Customers are instructed to examine their inventory, cease all distribution and quarantine affected product, and complete and return by email the response form included with the recall notice. Customers are to return any affected inventory via US Mail, marking the package, Attention: Returns Department Recall Product. The letter instructs customers identify and notify any customers the affected product was further distributed to.
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 noticePage updated: Jan 10, 2026