RecallHawk
Class I Recall

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

Bluegrass Ingredients Inc.

Summary

The FDA issued a Class I for Butter Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly lin by Bluegrass Ingredients Inc.. Reason: Positive Salmonella contamination.

Details

Source

Food Recall

External ID

H-0573-2026

Action Date

2026-03-25

Status

Terminated

Category

food

Product Description

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

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

Quantity Affected: 94 bags

Reason for Recall

Positive Salmonella contamination

Distribution

FL, IL, MD

Type: Voluntary: Firm initiated

Recall Initiated: 2026-02-26

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 48 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Bluegrass Ingredients Inc. has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Bluegrass Ingredients Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Bluegrass Ingredients Inc. have FDA actions?

Bluegrass Ingredients Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0573-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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