RecallRadar
FDA · FoodClass I

Lone Star Dairy Products LLC food recall: Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes

Salmonella

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
98582
Recall initiated
Mar 11, 2026
Classified by FDA
Mar 31, 2026
Posted in Enforcement Report
Apr 8, 2026
Terminated
Oct 1, 2026
Recalling firm
Lone Star Dairy Products LLC
Firm location
Canyon, TX, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
E-Mail
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Salmonella spp. identified in finished product testing

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Mar 11, 2026. FDA classified it 20 days later, on Mar 31, 2026. Distribution reported by FDA: USA

Recalled products (1)

  • H-0640-2026 Class I Terminated

    Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes

    Codes / lots: 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: 1,791,543.94 lbs

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 98582
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.