← FDA ENFORCEMENT
Z-1480-2026Class II

Staar Surgical AG

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Staar Surgical AG
Product type
Device
Status
Ongoing
Report date
2026-03-11
Distribution
International distribution to the countries of India, Iran, Korea, Saudi Arabia.
Firm state
N/A
Product quantity
7
Initiated by
Voluntary: Firm initiated
Reason for recall

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.

Product description

EVO+ Visian Toric Implantable Collamer Lens (TICL), Model: VTICM5

Code / lot info

UDI-DI: 00840311304363. Expiration Date: 2027-11-30 Serial Numbers: T2286964, T2286971, T2286973, T2286979, T2286980, T2286981, T2286988

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →