CLASS II ONGOING Food recall · Reported 1 Apr 2026 · FDA Enforcement Report

Bulk packaged Colustrum Powder recalled by Herbal Creations U

Herbal Creations U is recalling Bulk packaged Colustrum Powder. The recall was initiated on 29 Aug 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots: 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
Quantity recalled19,425 Kilograms

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0602-2026
FDA event ID
98462
Recalling firm
Herbal Creations U, Ontario, CA
Brand
Bulk
Classification
Class II
Status
Ongoing
Recall initiated
29 Aug 2025
FDA classified
20 Mar 2026
Reported
1 Apr 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Milk
Product category
Other

Timeline

29 Aug 2025Recall initiated by company
20 Mar 2026Classified by FDA+203 days
1 Apr 2026Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.

Product as listed by the FDA

Bulk packaged Colustrum Powder. packaged with generic product label.

Where it was distributed

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

Questions about this recall

Is Bulk packaged Colustrum Powder recalled?

Yes. Herbal Creations U recalled Bulk packaged Colustrum Powder on 29 Aug 2025. The recall is Class II and its status is Ongoing. Recall number H-0602-2026.

Why was it recalled?

Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.

Which lots are affected?

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

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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