RecallHawk
Class I Recall

Guilt Free No Sugar Added Ice Cream Homemade Vanilla 1.5qts

TH Searcy LLC

Summary

The FDA issued a Class I for Guilt Free No Sugar Added Ice Cream Homemade Vanilla 1.5qts by TH Searcy LLC. Reason: Undeclared Egg.

Details

Source

Food Recall

External ID

F-0408-2024

Action Date

2023-11-22

Status

Terminated

Category

food

Product Description

Guilt Free No Sugar Added Ice Cream Homemade Vanilla 1.5qts

Lot/Code Info: Lot 3135 BEST BY 11/15/2024, Lot 3136 BEST BY 11/16/2024, Lot 3216 BEST BY 02/04/2025

Quantity Affected: 5,750 Bundles (34,500 retail units)

Reason for Recall

Undeclared Egg

Distribution

Wholesale to 3 distributors: Walmart, Kroger, Associated Wholesale Grocers with retail distribution in Arkansas, Kansas, Kentucky, Louisiana, Mississippi, Missouri, Oklahoma, Tennessee, Texas.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-10-04

Company

TH Searcy LLC

Searcy, AR

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 145 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 (TH Searcy LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does TH Searcy LLC have FDA actions?

This is the only FDA action we have on record for TH Searcy LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0408-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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