Medical DeviceApr 14, 2021
Clerio Vision EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for daily wear recall — FDA Z-1352-2021
Contact lenses may be mislabeled with the incorrect lens power.
Class IIFDA: TerminatedClerio Vision
Recall history in this database
Classification mix: Class II: 2.
Medical DeviceJan 20, 2021
Clerio Vision, extreme H2O monthly, MED, DIA 14.0 PWR -2.25, UPC 675506803334 (6 count) and recall — FDA Z-0808-2021
One lot of contact lenses labeled as BC MED, DIA 14.0 PWR -2.25 contained BC MED, DIA 14.0, PWR -3.75 contact lenses
Class IIFDA: TerminatedClerio Vision
Understanding this recall history
This page summarizes recall records in which the official source identifies Clerio Vision as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.