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Home › FDA recalls › EVO+ Visian Toric Implantable Collamer Lens
CLASS II · ModerateFDA

Staar Surgical AG recalls EVO+ Visian Toric Implantable Collamer Lens

📅 Jan 21, 2026 · 📍 See notice
Recalling company
Staar Surgical AG
Product
EVO+ Visian Toric Implantable Collamer Lens (TICL), Model: VTICM5
Reason
Toric Implantable Collamer for correction/reduction of myopia in phakic eyes with astigmatism were labeled as 12.1 mm length but are 12.6 mm length lenses, so there is the potential for excessive vault, which may cause: Significant reduction of irido-corneal angles, Significant shallowing of anterior chamber, Patient discomfort, Elevated IOP/Angle closure, Unreactive pupil, Lens exchange/removal.
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
Jan 21, 2026
Reported
Mar 11, 2026
Distribution
International distribution to the countries of India, Iran, Korea, Saudi Arabia.
Status
Ongoing
Quantity
7
Lot / codes
UDI-DI: 00840311304363. Expiration Date: 2027-11-30 Serial Numbers: T2286964, T2286971, T2286973, T2286979, T2286980, T2286981, T2286988
Company location
Nidau, N/A
Recall type
Voluntary: Firm initiated
Recall number
Z-1480-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-1480-2026 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.