---
title: "Bulk packaged Colustrum Powder. packaged with generic product label. — FDA record H-0602-2026 | Is It on Recall"
description: "Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient."
url: https://isitonrecall.com/recall/fda-food-h-0602-2026-bulk-packaged-colustrum-powder-packaged-with-generic-product-label/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Bulk packaged Colustrum Powder. packaged with generic product label. — FDA record H-0602-2026

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 Aug 29, 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**: Bulk packaged Colustrum Powder. packaged with generic product label.
- **Reason**: Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.
- **Classification**: Class II
- **Recalling firm**: Herbal Creations USA
- **Quantity**: 19,425 Kilograms
- **Agency-reported status**: Ongoing
- **Source record identifier**: H-0602-2026

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0602-2026%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 | Lots: SSC40-2402 SWC15-2403; HCFCPDEX24006/01; HCFCPDEX24006/02; HCFCPDEX24006/04; HFCPDEX24006/05; HCFCPDEX24007/01; HCFCPDEX24008/03; HCFCPDEX24010/01; HCFCPDEX24010/02; HCFCPDEX24012/01; HCFCPDEX25001/01; HCFCPDEX25001/02; HCFCPDEX25005/01; HCFCPDEX25005/02; HCFCPDEX25005/03; HCFCPDEX25007/05; HCFCPDEX25007/06 |

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

## Distribution

Product is distributed to 30 US customers who receive and further process/package product prior to distribution.

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

## Dates in the source

- **Report date**: Apr 1, 2026
- **Recall initiation date**: Aug 29, 2025
- **Center classification date**: Mar 20, 2026

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/food/enforcement.json?search=recall_number%3A%22H-0602-2026%22)

## Related records

[Other food records](https://isitonrecall.com/category/other-food/) [Herbal Creations USA records](https://isitonrecall.com/brand/herbal-creations-usa/)
