RecallHawk
Class I Recall

Butter Buds Food Ingredients. Butter Buds 8X Non-Dairy LD, Item 49380. Sample Jars are 8 oz. and l lb. sized. White

Butter Buds Inc

Summary

The FDA issued a Class I for Butter Buds Food Ingredients. Butter Buds 8X Non-Dairy LD, Item 49380. Sample by Butter Buds Inc. Reason: Undeclared milk..

Details

Source

Food Recall

External ID

F-1307-2022

Action Date

2022-06-22

Status

Terminated

Category

food

Product Description

Butter Buds Food Ingredients. Butter Buds 8X Non-Dairy LD, Item 49380. Sample Jars are 8 oz. and l lb. sized. White poly jar with yellow cap

Lot/Code Info: Lot # 67122011 Best if used by: 1/11/23

Quantity Affected: 7 - one lb. jars and 7 - eight oz. jars

Reason for Recall

Undeclared milk.

Distribution

CA, CT, IL, MN, NC, OH, WA. Outside the US to Netherlands and Slovenia

Type: Voluntary: Firm initiated

Recall Initiated: 2022-05-11

Company

Butter Buds Inc

Racine, WI

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 175 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (Butter Buds Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Butter Buds Inc have FDA actions?

This is the only FDA action we have on record for Butter Buds Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1307-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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