FDA Recall of Bulk Packaged Colustrum Powder by Herbal Creations USA
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Herbal Creations USA is recalling 19,425 kilograms of bulk packaged Colustrum Powder due to the product label not declaring milk as an allergen, affecting specific lots distributed in the United States.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 7, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.
Recall of Bulk Packaged Colustrum Powder
What Happened
Herbal Creations USA is recalling bulk packaged Colustrum Powder because the product label does not declare Milk as an allergen ingredient.
Which Products Are Affected
The affected product is Bulk packaged Colustrum Powder, packaged with a generic product label. The quantity involved is 19,425 Kilograms. The specific lots affected are: 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, and HCFCPDEX25007/06. The product was distributed to 30 US customers who further process and package it prior to distribution in the United States. The official recall number is H-0602-2026.
What You Should Do
Consumers who have the affected product should check the lot numbers and follow the firm's initial notification, which was issued via letter, for further instructions on returns or refunds. Contact the recalling firm, Herbal Creations USA at 1001 S Doubleday Ave Unit F03, Ontario, CA 91761-1564, for more information.
Why This Matters
This recall addresses potential risks for individuals with milk allergies due to undeclared allergens, emphasizing the importance of accurate food labeling in preventing adverse health effects.
Source
FDA recall information, recall number H-0602-2026, available on the FDA website.
Original source: FDA Official Notice ↗
Related FDA Recalls
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Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,535 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to April 7, 2026.
Frequently Asked Questions
Common questions about this FDA recall.