---
title: "Eye and Ear Dropper, Product Code 67082 — FDA record Z-1702-2023 | Is It on Recall"
description: "Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb."
url: https://isitonrecall.com/recall/fda-device-z-1702-2023-eye-and-ear-dropper-product-code-67082/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Eye and Ear Dropper, Product Code 67082 — FDA record Z-1702-2023

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 Mar 30, 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**: Eye and Ear Dropper, Product Code 67082
- **Reason**: Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.
- **Classification**: Class II
- **Recalling firm**: Apothecary Products, LLC
- **Quantity**: 2,346 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1702-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1702-2023%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 | Lot Number: 030923; UPC Number: 025715670829 |

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

## Distribution

Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, HI, IL, IN, MO, NC, NJ, NY, OK, OR, PA, TN, TX, UT, WA and the country of Canada.

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**: Jun 21, 2023
- **Recall initiation date**: Mar 30, 2023
- **Center classification date**: Jun 9, 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-1702-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Apothecary Products, LLC records](https://isitonrecall.com/brand/apothecary-products-llc/)
