---
title: "Vetoquinol: FOLLTROPIN Injectable Kits for Cattle — FDA announcement Dec 2, 2025 | Is It on Recall"
description: "Presence of particulate matter"
url: https://isitonrecall.com/recall/fdapress-28d0b67453da28ab-vetoquinol-folltropin-injectable-kits-for-cattle/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Vetoquinol: FOLLTROPIN Injectable Kits for Cattle — FDA announcement Dec 2, 2025

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 Dec 2, 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**: FOLLTROPIN Injectable Kits for Cattle
- **Reason**: Presence of particulate matter
- **Classification**: Not supplied
- **Recalling firm**: Vetoquinol USA
- **Quantity**: Not supplied
- **Agency-reported status**: Company recall announcement
- **Source record identifier**: 28d0b67453da28ab

[Open the official record](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vetoquinol-usa-inc-recalls-six-lots-folltropin-injectable-kits-cattle-due-presence-particulate)

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | The Folltropin Kit consists of one 20 mL vial of Folltropin lyophilized FSH powder and one 20 mL vial of sterile bacteriostatic saline diluent. The Folltropin Kit is labeled with a lot number on the outside of the carton. The Folltropin powder and the sterile diluent are each labeled with a separate lot number on their respective vials.; Kit Lot # \| Diluent Lot # \| Expiration Date \| Distribution Begin Date \| Distribution End Date; 510578 \| 840915 \| 5/31/2026 \| 08/30/2023 \| 10/23/2023; 510579 \| 844585 \| 5/31/2026 \| 10/23/2025 \| 11/06/2023; 510580 \| 844583 \| 5/31/2026 \| 11/06/2023 \| 06/18/2024; 510581 \| 934975 \| 1/31/2027 \| 06/18/2024 \| 12/13/2024; 717059 \| 934976 \| 1/31/2027 \| 06/09/2025 \| 10/28/2025; 510582 \| 934973 \| 1/31/2027 \| 12/13/2024 \| 06/09/2025 |

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**

| Kit Lot # | Diluent Lot # | Expiration Date | Distribution Begin Date | Distribution End Date |
| --- | --- | --- | --- | --- |
| 510578 | 840915 | 5/31/2026 | 08/30/2023 | 10/23/2023 |
| 510579 | 844585 | 5/31/2026 | 10/23/2025 | 11/06/2023 |
| 510580 | 844583 | 5/31/2026 | 11/06/2023 | 06/18/2024 |
| 510581 | 934975 | 1/31/2027 | 06/18/2024 | 12/13/2024 |
| 717059 | 934976 | 1/31/2027 | 06/09/2025 | 10/28/2025 |
| 510582 | 934973 | 1/31/2027 | 12/13/2024 | 06/09/2025 |

Announcement retrieved Oct 1, 2026. [Official announcement](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vetoquinol-usa-inc-recalls-six-lots-folltropin-injectable-kits-cattle-due-presence-particulate).

## Distribution

Not supplied

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

## Dates in the source

- **Fda listing date**: Dec 2, 2025
- **Company announcement date**: Nov 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

Customers who have received FOLLTROPIN Kits from the batches impacted by this recall should stop using the product immediately and quarantine product subject to recall. Please contact Vetoquinol USA, Inc. for further instructions for returning or disposal of the recall product. Consumers with questions regarding this company announcement should call Vetoquinol USA, Inc. at 1-800-267-5707 Monday through Friday between the hours of 8 a.m. and 5 p.m. Central Standard Time.

[Read the current instructions](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vetoquinol-usa-inc-recalls-six-lots-folltropin-injectable-kits-cattle-due-presence-particulate)

## Related records

[Other consumer products records](https://isitonrecall.com/category/other-consumer-products/) [Vetoquinol USA records](https://isitonrecall.com/brand/vetoquinol-usa/)