CLASS I ONGOING Food recall · Reported 13 May 2026 · FDA Enforcement Report

Buttermilk Powder - (packed under 1 label: BMP Extra Grade Standard) recalled

California Dairies is recalling Buttermilk Powder - (packed under 1 label: BMP Extra Grade Standard). The recall was initiated on 20 Apr 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBatch Codes for recalled product all start with A or B full list below. Batch Codes and Production Date: A22525-08-A 8/13/2025; A22525-08-B 8/13/2025; A22525-08-C 8/13/2025; A22525-08-D 8/13/2025; A22525-08-E 8/13/2025; A22525-08-F 8/13/2025; A22525-08-G 8/13/2025; A22525-08-H 8/13/2025.
Quantity recalled19,841 lbs.

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-0700-2026
FDA event ID
98796
Recalling firm
California Dairies, Visalia, CA
Classification
Class I
Status
Ongoing
Recall initiated
20 Apr 2026
FDA classified
5 May 2026
Reported
13 May 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Salmonella
Product category
Other

Timeline

20 Apr 2026Recall initiated by company
5 May 2026Classified by FDA+15 days
13 May 2026Published in enforcement report+8 days

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

Reason for recall

Potential contamination with Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Buttermilk Powder - paper bags 25 kg. (packed under 1 label: BMP Extra Grade Standard)

Where it was distributed

U.S. Distribution: Unknown and to be determined during RAC assignment. Domestic consignees pick-up product from CDI. Foreign Distribution: Mexico, Philippines, Dominican Republic.

Questions about this recall

Why was it recalled?

Potential contamination with Salmonella.

Which lots are affected?

Batch Codes for recalled product all start with A or B full list below. Batch Codes and Production Date: A22525-08-A 8/13/2025; A22525-08-B 8/13/2025; A22525-08-C 8/13/2025; A22525-08-D 8/13/2025; A22525-08-E 8/13/2025; A22525-08-F 8/13/2025; A22525-08-G 8/13/2025; A22525-08-H 8/13/2025.

Where was it sold?

U.S. Distribution: Unknown and to be determined during RAC assignment. Domestic consignees pick-up product from CDI. Foreign Distribution: Mexico, Philippines, Dominican Republic.

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 98796

This product is part of a recall event; the main page for the event is Low Heat Non-Fat Dried Milk Powder - (packed under 5 labels recalled.

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