RecallHawk
Class II Recall

Premium Food Bubble Gum, packed in 2.5 oz clear flexible plastic packaging, all lots and codes. Sold in unit case of 30

Bader Enterprises, Inc.

Summary

The FDA issued a Class II for Premium Food Bubble Gum, packed in 2.5 oz clear flexible plastic packaging, all by Bader Enterprises, Inc.. Reason: Contains undeclared colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake)..

Details

Source

Food Recall

External ID

H-0539-2026

Action Date

2026-03-11

Status

Ongoing

Category

food

Product Description

Premium Food Bubble Gum, packed in 2.5 oz clear flexible plastic packaging, all lots and codes. Sold in unit case of 30 LB.

Lot/Code Info: Lot/Unit Numbers: 13 BEST BY : DEC-2028 UPC Codes: 015747199269

Quantity Affected: 400 lbs.

Reason for Recall

Contains undeclared colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).

Distribution

NJ, NY

Type: Voluntary: Firm initiated

Recall Initiated: 2026-01-16

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

Bader Enterprises, Inc. has 2 FDA actions in our database, including 2 recalls.

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

How often does Bader Enterprises, Inc. have FDA actions?

Bader Enterprises, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0539-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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