RecallHawk
Class I Recall

United Dairy Farmers - Holiday Nogg packaged in clear plastic HDPR 1/2 gallon jug. UPC: 076310050493

United Dairy Farmers Inc

Summary

The FDA issued a Class I for United Dairy Farmers - Holiday Nogg packaged in clear plastic HDPR 1/2 gallon ju by United Dairy Farmers Inc. Reason: Undeclared Allergen - Egg.

Details

Source

Food Recall

External ID

F-0642-2024

Action Date

2023-12-27

Status

Terminated

Category

food

Product Description

United Dairy Farmers - Holiday Nogg packaged in clear plastic HDPR 1/2 gallon jug. UPC: 076310050493

Lot/Code Info: Batch Number: 21-65 13:41 BB 12/19/2023 Lot No 21-65 Product No 7631005049 Packer/Manufacturer No 21-65 Best By 12/19/23

Quantity Affected: 3057 units

Reason for Recall

Undeclared Allergen - Egg

Distribution

Ohio, Kentucky, and Indiana

Type: Voluntary: Firm initiated

Recall Initiated: 2023-12-06

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

How often does United Dairy Farmers Inc have FDA actions?

This is the only FDA action we have on record for United Dairy Farmers Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0642-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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