RecallHawk
Class II Recall

Dole Apple Juice (primary package), 15.2 Fl oz., PET, 12 bottles per case, Refrigerate after opening

TROPICANA BRANDS GROUP

Summary

The FDA issued a Class II for Dole Apple Juice (primary package), 15.2 Fl oz., PET, 12 bottles per case, Refri by TROPICANA BRANDS GROUP. Reason: A manufacturing process deviation occurred which may cause spoilage or microbial contamination and affect shelf stability..

Details

Source

Food Recall

External ID

H-0073-2026

Action Date

2025-10-22

Status

Terminated

Category

food

Product Description

Dole Apple Juice (primary package), 15.2 Fl oz., PET, 12 bottles per case, Refrigerate after opening

Lot/Code Info: Case Code: Jan 10 26 xxxx(military time) ET 1 Primary Package code: (first line) Jan 10 26 CT127 (second line) XXXX (military time) ET071452

Quantity Affected: 1,599 cases

Reason for Recall

A manufacturing process deviation occurred which may cause spoilage or microbial contamination and affect shelf stability.

Distribution

The adulterated product was distributed to the following states: AR, CO, IA, KS, NE, MO, TX, MS, TN, NM, OK,

Type: Voluntary: Firm initiated

Recall Initiated: 2025-09-11

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 75 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 (TROPICANA BRANDS GROUP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does TROPICANA BRANDS GROUP have FDA actions?

This is the only FDA action we have on record for TROPICANA BRANDS GROUP in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0073-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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