Severity
Moderate
FDA Food recall · Reported April 1, 2026
Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.
Herbal Creations USA recalled Bulk packaged Colustrum Powder. packaged with generic product label. - a moderate-severity action.
Bulk packaged Colustrum Powder. packaged with generic product label. was recalled by Herbal Creations USA in April 1, 2026. Reason: Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.. Check the official notice for the remedy. Verify recall #H-0602-2026 with the FDA Food before acting.
The recall
Herbal Creations USA issued this moderate-severity FDA Food recall-Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient..
Sourced from official FDA Food enforcement records. Verify recall #H-0602-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #H-0602-2026) was formally reported on April 1, 2026, with the manufacturer initiating the action on August 29, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. Herbal Creations USA is listed as the recalling firm, operating out of Ontario, CA. Federal records list the affected scope as 19,425 Kilograms.
The documented reason for this recall is: Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient. Distribution data in the federal record shows the product reached: Product is distributed to 30 US customers who receive and further process/package product prior to distribution.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
19,425 Kilograms
Related Recalls
6
6 from same agency
Bulk packaged Colustrum Powder. packaged with generic product label.
Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | H-0602-2026 |
| Date reported | April 1, 2026 |
| Date initiated | August 29, 2025 |
| Recalling firm | Herbal Creations USA |
| Firm location | Ontario, CA |
| Affected scope | 19,425 Kilograms |
| Distribution | Product is distributed to 30 US customers who receive and further process/package product prior to distribution. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Winder Laboratories, LLC · 2026-03-25
Imu-Tek Animal Health, Incorporated · 2026-02-11
Fazt & Loud LLC · 2026-02-11
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported April 1, 2026. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.