---
title: "Fendall 2000: Non-Sterile Eyewash Cartridge — FDA announcement Apr 5, 2024 | Is It on Recall"
description: "Non-compliance with current good manufacturing practice (cGMP) requirements."
url: https://isitonrecall.com/recall/fdapress-47a0432d10d6a326-fendall-2000-non-sterile-eyewash-cartridge/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA company announcement

# Fendall 2000: Non-Sterile Eyewash Cartridge — FDA announcement Apr 5, 2024

Published notice; closure not supplied

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Apr 5, 2024. 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**: Non-Sterile Eyewash Cartridge
- **Reason**: Non-compliance with current good manufacturing practice (cGMP) requirements.
- **Classification**: Not supplied
- **Recalling firm**: Honeywell Safety Products USA
- **Quantity**: Not supplied
- **Agency-reported status**: Company recall announcement
- **Source record identifier**: 47a0432d10d6a326

[Open the official record](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/honeywell-safety-products-usa-inc-issues-voluntary-worldwide-recall-honeywell-fendall-2000-non)

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Product and Distribution Information Table; Product Name \| Manufacturer’s Product Number/ Catalog Number \| Manufacturing Dates (DD/MMM/YYYY) \| Expiration Date (DD/MMM/YYYY) \| Region \| Quantity; Fendall 2000 Non-Sterile Eyewash Cartridge \| 32-002050-0000 \| 11-Oct- 2021 through 21-Jun-2023 \| 11-Oct-2023 through 21-Jun-2025 \| USA \| 6,954; Fendall 2000 Non-Sterile Eyewash Cartridge \| 32-002050-0000 \| 11-Oct- 2021 through 21-Jun-2023 \| 11-Oct-2023 through 21-Jun-2025 \| Canada \| 3,651 |

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

## Product tables from the announcement

These identifying details come from the company announcement posted by FDA. Check the current notice for revisions.

**FDA company announcement, table 1**

| Product and Distribution Information Table | Product and Distribution Information Table | Product and Distribution Information Table | Product and Distribution Information Table | Product and Distribution Information Table | Product and Distribution Information Table |
| --- | --- | --- | --- | --- | --- |
| Product Name | Manufacturer’s Product Number/ Catalog Number | Manufacturing Dates (DD/MMM/YYYY) | Expiration Date (DD/MMM/YYYY) | Region | Quantity |
| Fendall 2000 Non-Sterile Eyewash Cartridge | 32-002050-0000 | 11-Oct- 2021 through 21-Jun-2023 | 11-Oct-2023 through 21-Jun-2025 | USA | 6,954 |
| Fendall 2000 Non-Sterile Eyewash Cartridge | 32-002050-0000 | 11-Oct- 2021 through 21-Jun-2023 | 11-Oct-2023 through 21-Jun-2025 | Canada | 3,651 |

Announcement retrieved Oct 1, 2026. [Official announcement](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/honeywell-safety-products-usa-inc-issues-voluntary-worldwide-recall-honeywell-fendall-2000-non).

## Distribution

Not supplied

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

## Dates in the source

- **Fda listing date**: Apr 5, 2024
- **Company announcement date**: Apr 4, 2024

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

Customers with questions regarding this recall can contact Honeywell Safety Products USA, Inc. by telephone USA 1-800-430-5490, Canada 1-888-212-7233 or CustomerServiceInquiryBox@Honeywell.com between the hours of 8:00AM to 4:00PM EST. Customers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this eyewash solution.

[Read the current instructions](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/honeywell-safety-products-usa-inc-issues-voluntary-worldwide-recall-honeywell-fendall-2000-non)

## Before changing a medicine

Follow urgent instructions in the current official recall notice. Speak to your pharmacist or prescriber before stopping or changing a prescribed medicine.

Talk to your doctor or pharmacist if you have questions or concerns about your medicine. [FDA medication recall guidance](https://www.fda.gov/drugs/drug-recalls/understanding-drug-recalls-what-know-and-what-do)

## Related records

[Medications records](https://isitonrecall.com/category/medications/) [Honeywell Safety Products USA records](https://isitonrecall.com/brand/honeywell-safety-products-usa/)