The FDA has posted 5 enforcement recalls of (disposable) contact lens devices since 2025, none of them Class I (most serious). Most recent report: Sep 30, 2026.
A small number of lenses within the affected lot are of the incorrect power.
One lot manufactured with an invalid sterilization cycle.
One lot manufactured with an invalid sterilization cycle.
One lot manufactured with an invalid sterilization cycle.
a limited number of lots were manufactured with an incorrect cylinder power.
Source: U.S. FDA openFDA device enforcement reports, updated continuously. Device type per the FDA's RES classification (“Lens, Contact, (Disposable)”). Informational only — verify against the FDA before acting.