RecallHawk
Class III Recall

Calais Brand Grape jelly; 128 FL. OZ. (1 GAL.) 3.785 L; INGREDIENTS: Grape Juice, Corn Syrup, High Fructose Corn Syrup,

Elwood International, Inc.

Summary

The FDA issued a Class III for Calais Brand Grape jelly; 128 FL. OZ. (1 GAL.) 3.785 L; INGREDIENTS: Grape Juice by Elwood International, Inc.. Reason: Contains undeclared colors (FD&C Blue 1 and FD&C Red 40).

Details

Source

Food Recall

External ID

H-0252-2025

Action Date

2025-07-16

Status

Terminated

Category

food

Product Description

Calais Brand Grape jelly; 128 FL. OZ. (1 GAL.) 3.785 L; INGREDIENTS: Grape Juice, Corn Syrup, High Fructose Corn Syrup, Pectin, Citric Acid; REFRIGERATE AFTER OPENING; UPC 040264 10128 0

Lot/Code Info: Model, catalog, or product order numbers: W-101-28 UPC 040264101280

Quantity Affected: 43 cases

Reason for Recall

Contains undeclared colors (FD&C Blue 1 and FD&C Red 40)

Distribution

NY, NJ

Type: Voluntary: Firm initiated

Recall Initiated: 2025-02-19

Company

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 147 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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

How often does Elwood International, Inc. have FDA actions?

This is the only FDA action we have on record for Elwood International, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0252-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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