---
title: "Alcon Custom-Pak, Surgical Procedure Pack REF 14057-09, 45K W/DUOVISC CATARAC... — FDA record Z-0260-2024 | Is It on Recall"
description: "Custom surgical procedure packs contain latex gloves but are labeled as \"latex free\"."
url: https://isitonrecall.com/recall/fda-device-z-0260-2024-alcon-custom-pak-surgical-procedure-pack-ref-14057-09-45k-w-duovisc-cataract-n-virginia-eye-surg-ctr/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Alcon Custom-Pak, Surgical Procedure Pack REF 14057-09, 45K W/DUOVISC CATARACT, N VIRGINIA EYE SURG CTR — FDA record Z-0260-2024

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 7, 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**: Alcon Custom-Pak, Surgical Procedure Pack REF 14057-09, 45K W/DUOVISC CATARACT, N VIRGINIA EYE SURG CTR
- **Reason**: Custom surgical procedure packs contain latex gloves but are labeled as "latex free".
- **Classification**: Class II
- **Recalling firm**: Alcon Research, LLC
- **Quantity**: 120 packs
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0260-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0260-2024%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 | LOT # : 160NMU, UDI: (01)10380653302278 |

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

## Distribution

US: VA OUS: None

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

- [Virginia](https://isitonrecall.com/state/virginia/)

## Dates in the source

- **Report date**: Nov 15, 2023
- **Recall initiation date**: Sep 7, 2023
- **Center classification date**: Nov 7, 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-0260-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Alcon Research, LLC records](https://isitonrecall.com/brand/alcon-research-llc/)