RecallRadar
High RiskReported March 25, 2026

Butter-Rich Powder, Net Weight 50 LB.

Recalled by Bluegrass Ingredients Inc.

Food recall

Bluegrass Ingredients Inc.

Class I — most serious

There is a reasonable chance that using this product could cause serious health problems or death.

See all recalls involving Salmonella

Bluegrass Ingredients Inc. has recalled Butter-Rich Powder, Net Weight 50 LB., according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on March 25, 2026 and was initiated on February 26, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Butter-Rich Powder, Net Weight 50 LB., with approximately 99 bags affected. The company behind the recall is Bluegrass Ingredients Inc., based in Springfield, KY. The FDA describes the product as: “Butter-Rich Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner”

Why was Butter-Rich Powder, Net Weight 50 LB. recalled?

According to the FDA, the stated reason for the recall is: “Potential Salmonella contamination.” In plain terms, this recall relates to Salmonella.

Salmonella is a group of bacteria that is one of the most common causes of foodborne illness in the United States. Public health authorities note that infections can lead to symptoms such as fever, diarrhea, and stomach cramps, and that young children, older adults, and people with weakened immune systems are at higher risk of serious illness. Because it can spread through contaminated food, regulators treat Salmonella findings seriously.

What should you do?

If you think you may have bought Butter-Rich Powder, Net Weight 50 LB., compare it against the product description and identifying codes (Product Number: BDF0006B, Lot: 6018, Best By: 1/18/2027) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Bluegrass Ingredients Inc. or your local health authority.

About this recall

This recall was distributed in KY. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Terminated
Date reported
March 25, 2026
Recall started
February 26, 2026
Distributed in
KY
What was recalled
Butter-Rich Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner
Why it was recalled (as stated by the FDA)
Potential Salmonella contamination
How to identify the affected product
Product Number: BDF0006B, Lot: 6018, Best By: 1/18/2027
Amount recalled
99 bags

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Butter-Rich Powder, Net Weight 50 LB. recalled?+

According to the FDA: Potential Salmonella contamination

How serious is this recall?+

Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.

What should I do if I have Butter-Rich Powder, Net Weight 50 LB.?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0572-2026. Information last synced from the FDA on July 6, 2026.

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