Class ITerminatedVoluntary: Firm initiated
Bluegrass Ingredients Inc.: food recall H-0573-2026
Bluegrass Ingredients Inc. of Springfield, KY recalled Butter Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner. Reason: Positive Salmonella contamination. The FDA listed it as Class I in its Enforcement Report dated Mar 25, 2026; distribution: Florida, Illinois, Maryland.
Record status as published: Terminated (terminated Jun 17, 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
- Butter Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner
- Product quantity
- 94 bags
- Reason for recall
- Positive Salmonella contamination
- Codes, lots and dates on the package
- Product Number: BDF0006, Lot: 6018, Best By: 1/18/2027
- Distribution pattern
- FL, IL, MD
- Recalling firm
- Bluegrass Ingredients Inc., Springfield, KY
- 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
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Feb 26, 2026 |
| Classified by the FDA | Mar 17, 2026 |
| Published in the Enforcement Report | Mar 25, 2026 |
| Terminated | Jun 17, 2026 |
Other products in the same recall event
The FDA groups related products under one recall event (event 98546).
- H-0572-2026 — Butter-Rich Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner
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OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0573-2026 (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.