---
title: "EVO+VISIAN Implantable Collamer Lens, REF: VTICM5_12.6. Phakic Toric Intraocu... — FDA record Z-0471-2024 | Is It on Recall"
description: "Their is a potential that intraocular implant devices may not meet specifications."
url: https://isitonrecall.com/recall/fda-device-z-0471-2024-evo-visian-implantable-collamer-lens-ref-vticm5-12-6-phakic-toric-intraocular-lens/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# EVO+VISIAN Implantable Collamer Lens, REF: VTICM5\_12.6. Phakic Toric Intraocular lens. — FDA record Z-0471-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 29, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: EVO+VISIAN Implantable Collamer Lens, REF: VTICM5\_12.6. Phakic Toric Intraocular lens.
- **Reason**: Their is a potential that intraocular implant devices may not meet specifications.
- **Classification**: Class II
- **Recalling firm**: Staar Surgical Company
- **Quantity**: 15 UNITS
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0471-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0471-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | T1210975/ (01)00841542114141(11)221015(17)240930(21)T1210975; T1283082/ (01)00841542115506(11)221212(17)241130(21)T1283082; T1359541/ (01)00841542115544(11)230210(17)250131(21)T1359541; T1377771/ (01)00841542115469(11)230223(17)250131(21)T1377771; T1443561/ (01)00841542115537(11)230403(17)250331(21)T1443561; T1226995/ (01)00841542114615(11)221029(17)240930(21)T1226995; T1365648/ (01)00841542115506(11)230214(17)250131(21)T1365648; T1255982/ (01)00841542115247(11)221120(17)241031(21)T1255982; T1555552/ (01)00841542114776(11)230621(17)250531(21)T1555552; T1187773/ (01)00841542115209(11)220926(17)240831(21)T1187773; T1235414/ (01)00841542114530(11)221106(17)241031(21)T1235414; T1210808/ (01)00841542114349(11)221015(17)240930(21)T1210808; T1195554/ (01)00841542115384(11)221003(17)240930(21)T1195554; T1373152/ (01)00841542114981(11)230220(17)250131(21)T1373152; T1566889/ (01)00841542114950(11)230629(17)250531(21)T1566889 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: AR AZ CA CO CT FL GA HI ID IL IN KS KY LA MA MD MI MN MO MT NC ND NE NJ NV NY OH OK OR PA SC SD TN TX UT VA WA WI OUS: None

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Dec 13, 2023
- **Recall initiation date**: Sep 29, 2023
- **Center classification date**: Dec 1, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0471-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Staar Surgical Company records](https://isitonrecall.com/brand/staar-surgical-company/)
