RecallHawk
Class II Recall

Beverage Base Lemonade, 3 gallon, BIB: Best By 12/12/2025; Beverage Base Lemonade, 5 gallon, BIB: Best By 01/12/2026

OCBW INC

Summary

The FDA issued a Class II for Beverage Base Lemonade, 3 gallon, BIB: Best By 12/12/2025; Beverage Base Lemonad by OCBW INC. Reason: Undeclared Yellow #5.

Details

Source

Food Recall

External ID

F-0574-2025

Action Date

2025-03-05

Status

Ongoing

Category

food

Product Description

Beverage Base Lemonade, 3 gallon, BIB: Best By 12/12/2025; Beverage Base Lemonade, 5 gallon, BIB: Best By 01/12/2026

Lot/Code Info: Best By 12/12/2025 Best by 1/12/2026

Quantity Affected: 8,847 Units Total

Reason for Recall

Undeclared Yellow #5

Distribution

Texas, Colorado, New Mexico, Kentucky, Oklahoma, Missouri, Arkansas, California

Type: Voluntary: Firm initiated

Recall Initiated: 2025-01-31

Company

OCBW INC

Dallas, TX

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

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

How often does OCBW INC have FDA actions?

OCBW 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 "F-0574-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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