---
title: "TECNIS Symfony, Extended Range of Vision IOL, REF: ZXR00, STERILE.EO, Rx Only — FDA record Z-2288-2023 | Is It on Recall"
description: "Their is a potential that intraocular lenses (IOLs) were manufactured with unintended toric fiducial marks."
url: https://isitonrecall.com/recall/fda-device-z-2288-2023-tecnis-symfony-extended-range-of-vision-iol-ref-zxr00-sterile-eo-rx-only/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# TECNIS Symfony, Extended Range of Vision IOL, REF: ZXR00, STERILE.EO, Rx Only — FDA record Z-2288-2023

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 Jul 6, 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**: TECNIS Symfony, Extended Range of Vision IOL, REF: ZXR00, STERILE.EO, Rx Only
- **Reason**: Their is a potential that intraocular lenses (IOLs) were manufactured with unintended toric fiducial marks.
- **Classification**: Class II
- **Recalling firm**: Johnson & Johnson Surgical Vision, Inc.
- **Quantity**: 42
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2288-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2288-2023%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: 5050474579163/ Serial Numbers: 8210142244, 8210152244, 8210162244, 8210172244, 8210182244, 8210192244, 8210202244, 8210212244, 8210222244, 8210232244, 8210242244, 8210252244, 8210262244, 8210272244, 8210282244, 8210292244, 8210302244, 8210312244, 8210322244, 8210332244, 8210342244, 8210352244, 8210362244, 8210372244, 8210382244, 8210392244, 8210402244, 8210412244, 8210422244, 8210432244, 8210442244, 8210452244, 8210462244, 8210472244, 8210482244, 8210492244, 8210502244, 8210512244, 8210522244, 8210532244, 8210542244, 8210552244, |

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

## Distribution

International distribution to the countries of China, India, Korea.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Aug 9, 2023
- **Recall initiation date**: Jul 6, 2023
- **Center classification date**: Aug 3, 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-2288-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Johnson & Johnson Surgical Vision Inc records](https://isitonrecall.com/brand/johnson-johnson-surgical-vision-inc/)