Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1352-2021 — 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

U.S. FDA — Device Enforcement · United States · 2021-02-16 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1352-2021
Date of alert: 2021-02-16
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Clerio Vision
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 0114511565

Reported risk: Contact lenses may be mislabeled with the incorrect lens power.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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