Class ITerminatedVoluntary: Firm initiated
Lone Star Dairy Products LLC: food recall H-0640-2026
Lone Star Dairy Products LLC of Canyon, TX recalled Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes. Reason: Salmonella spp. identified in finished product testing. The FDA listed it as Class I in its Enforcement Report dated Apr 8, 2026.
Record status as published: Terminated (terminated Oct 1, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes
- Product quantity
- 1,791,543.94 lbs
- Reason for recall
- Salmonella spp. identified in finished product testing
- Codes, lots and dates on the package
- 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.
- Distribution pattern
- USA
- Recalling firm
- Lone Star Dairy Products LLC, Canyon, TX
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Mar 11, 2026 |
| Classified by the FDA | Mar 31, 2026 |
| Published in the Enforcement Report | Apr 8, 2026 |
| Terminated | Oct 1, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0640-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.