CLASS I Food recall · Reported 18 Jun 2025 · FDA Enforcement Report

Non Fat Dry Milk recalled by Crystal Creamery

Crystal Creamery is recalling Non Fat Dry Milk, distributed in California, Texas. The recall was initiated on 19 May 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot: 21APR25 Internal Item Number: 79065
Quantity recalled92,594 lbs (1,680 bags - 25kg/bag)

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-0097-2025
FDA event ID
96971
Recalling firm
Crystal Creamery, Modesto, CA
Brand
Non
Classification
Class I
Status
Terminated
Recall initiated
19 May 2025
FDA classified
25 Jun 2025
Reported
18 Jun 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Salmonella
Product category
Milk

Timeline

19 May 2025Recall initiated by company
18 Jun 2025Published in enforcement report+30 days
25 Jun 2025Classified by FDA+7 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

NON FAT DRY MILK. "LOW HEAT SPRAY PROCESS GRADE A NON FAT DRY MILK MADE FROM PASTERUIZED MILK, NET WEIGHT 25.00 KG, PRODUCT OF U.S.A."

Where it was distributed

CA and TX

CaliforniaTexas

Questions about this recall

Why was it recalled?

Potential contamination with Salmonella.

Which lots are affected?

Lot: 21APR25 Internal Item Number: 79065

Where was it sold?

CA and TX

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.

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