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

Recall Z-3310-2024 — BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia with astigmatism) with presbyopia in aphakic and non-aphakic persons.

U.S. FDA — Device Enforcement · United States · 2024-08-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3310-2024
Date of alert
2024-08-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
CooperVision, Inc.
Product category
device
Product type
Devices
Reported risk: Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
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.

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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.