Summary
The FDA issued a Class I for Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes by Lone Star Dairy Products LLC. Reason: Salmonella spp. identified in finished product testing.
Details
Source
Food Recall
External ID
H-0640-2026
Action Date
2026-04-08
Status
Ongoing
Category
food
Product Description
Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes
Lot/Code Info: NFDM Low Heat, NFDM High Heat, and SMP Medium Heat Lot Codes : 26015B; 26016B; 26017B; 26018B; 26019B; 26022B; 26023B; 26024B; 26024BT; 26025B; 26025BT; 26026B; 26027B; 26028B; 26029B; 26030B; 26034B; 26035B; 26040B; 26041B; 26041BT; 26042B; 26042BT; 26043B; 26044B; 26046BT; 26047BT; 26048BT. The products were packaged in 25 kg bags or 1 metric ton totes.
Quantity Affected: 1,791,543.94 lbs
Reason for Recall
Salmonella spp. identified in finished product testing
Distribution
USA
Type: Voluntary: Firm initiated
Recall Initiated: 2026-03-11
Company
Canyon, TX
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 59 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lone Star Dairy Products LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lone Star Dairy Products LLC have FDA actions?
This is the only FDA action we have on record for Lone Star Dairy Products LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0640-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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