---
title: "Akreos, SKU: AO60P0300. Akreos intraocular lenses — FDA record Z-2451-2025 | Is It on Recall"
description: "An off-power error was identified, which resulted in a diopter of 16, rather than the intended 3 diopter. Implantation of affected intraocular lens could result"
url: https://isitonrecall.com/recall/fda-device-z-2451-2025-akreos-sku-ao60p0300-akreos-intraocular-lenses/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Akreos, SKU: AO60P0300. Akreos intraocular lenses — FDA record Z-2451-2025

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 Jun 6, 2025. 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**: Akreos, SKU: AO60P0300. Akreos intraocular lenses
- **Reason**: An off-power error was identified, which resulted in a diopter of 16, rather than the intended 3 diopter. Implantation of affected intraocular lens could result in functional visual impairment or reduction in visual acuity which could result in the need for optical or surgical correction.
- **Classification**: Class III
- **Recalling firm**: Bausch & Lomb Surgical, Inc.
- **Quantity**: 2
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2451-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2451-2025%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 | UDI-DI: 10757770501783, Lot: 1Q29212, Serial Numbers: 1Q29212006 and 1Q29212010 |

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

## Distribution

US: AZ, CA

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

- [Arizona](https://isitonrecall.com/state/arizona/)
- [California](https://isitonrecall.com/state/california/)

## Dates in the source

- **Report date**: Sep 3, 2025
- **Recall initiation date**: Jun 6, 2025
- **Center classification date**: Aug 26, 2025

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-2451-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Bausch & Lomb Surgical, Inc. records](https://isitonrecall.com/brand/bausch-lomb-surgical-inc/)