Official recall record
enVista® Hydrophobic Acrylic IOL
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-04-02
- Last updated (per notice)
- 2025-04-28
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Products are being voluntary recalled out of an abundance of caution based on an increase in the number of Toxic Anterior Segment Syndrome (TASS) cased detected in complaints. Users should immediately stop implanting the affected IOL models. Only certain IOL lots manufactured from September 2024 to March 2025 are impacted. No other Bausch + Lomb products or lots distributed in Canada are impacted by this recall. Recall start date: March 28, 2025
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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