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Class I: serious health riskTerminated

Bluegrass Ingredients Butter Powder Recall

Butter Powder

Bluegrass Ingredients Inc. · Springfield, KY

Risk level
Class I
Reported by FDA
Mar 25, 2026
Recall ID
H-0573-2026
Check your lot numberHow we source this data

Summary

Bluegrass Ingredients recalled Butter Powder starting Feb 26, 2026. The FDA classified it as Class I (serious health risk) and published enforcement report H-0573-2026 on Mar 25, 2026. Reason: Positive Salmonella contamination. Status: Terminated.

Why it was recalled

Positive Salmonella contamination

Product description

Butter Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner

Lot numbers, UPCs & expiration codes

Product Number: BDF0006, Lot: 6018, Best By: 1/18/2027

Where it was sold

FL, IL, MD

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-0573-2026
Classification
Class I
Status
Terminated
Recall initiated
Feb 26, 2026
FDA report date
Mar 25, 2026
Quantity
94 bags
Recall type
Voluntary: Firm initiated
Recalling firm
Bluegrass Ingredients Inc.

Original FDA data

Every field from FDA enforcement report H-0573-2026, exactly as published.

Show all FDA fields
City
Springfield
State
KY
Status
Terminated
Country
United States
Event ID
98546
Address
606 W Main St
Code information
Product Number: BDF0006, Lot: 6018, Best By: 1/18/2027
Postal code
40069-1275
Report date
Mar 25, 2026
Product type
Food
Recall number
H-0573-2026
Classification
Class I
Recalling firm
Bluegrass Ingredients Inc.
Product quantity
94 bags
Termination date
Jun 17, 2026
Reason for recall
Positive Salmonella contamination
Voluntary / mandated
Voluntary: Firm initiated
Product description
Butter Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner
Distribution pattern
FL, IL, MD
Recall initiation date
Feb 26, 2026
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Mar 17, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0573-2026, published Mar 25, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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