RecallHawk
Class II Recall

CHILE VERDE EGG BITES; NET WT. 4.6 OZ (130 g); 2 egg bites/package

Valley Fine Foods Co., Inc

Summary

The FDA issued a Class II for CHILE VERDE EGG BITES; NET WT. 4.6 OZ (130 g); 2 egg bites/package by Valley Fine Foods Co., Inc. Reason: Potential contamination with foreign materials..

Details

Source

Food Recall

External ID

F-0746-2025

Action Date

2025-05-07

Status

Ongoing

Category

food

Product Description

CHILE VERDE EGG BITES; NET WT. 4.6 OZ (130 g); 2 egg bites/package

Lot/Code Info: UPC code: 0-41220-30655-8; Lot: 05/17/25 [time stamp] L2

Quantity Affected: 646 cases (7 packages/case)

Reason for Recall

Potential contamination with foreign materials.

Distribution

TX

Type: Voluntary: Firm initiated

Recall Initiated: 2025-04-03

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 34 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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

How often does Valley Fine Foods Co., Inc have FDA actions?

This is the only FDA action we have on record for Valley Fine Foods Co., Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0746-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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