Class IIOngoingVoluntary: Firm initiated
Herbal Creations USA: food recall H-0602-2026
Herbal Creations USA of Ontario, CA recalled 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. The FDA listed it as Class II in its Enforcement Report dated Apr 1, 2026.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Bulk packaged Colustrum Powder. packaged with generic product label.
- Product quantity
- 19,425 Kilograms
- Reason for recall
- Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.
- Codes, lots and dates on the package
- 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
- Distribution pattern
- Product is distributed to 30 US customers who receive and further process/package product prior to distribution.
- Recalling firm
- Herbal Creations USA, Ontario, CA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Letter
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Aug 29, 2025 |
| Classified by the FDA | Mar 20, 2026 |
| Published in the Enforcement Report | Apr 1, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0602-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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