Recall Radar

Tropicana Brands Group recalls Dole Apple Juice: contamination

October 22, 2025 · Tropicana Brands Group Class II

Class IIFDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Reason for the recallA manufacturing process deviation occurred which may cause spoilage or microbial contamination and affect shelf stability.

Find the official FDA enforcement report

Recall at a glance

Recalling company
Tropicana Brands Group
Location
Chicago, IL
Reported by FDA
October 22, 2025
Recall started
September 11, 2025
Risk class
Class II
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Beverages
Reason type
Other contaminationLabeling and quality

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • Dole Apple Juice (primary package), 15.2 Fl oz., PET, 12 bottles per case, Refrigerate after opening
    Quantity: 1,599 cases
    Codes: 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

Where it was distributed

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

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

Tropicana Brands Group recalled 1 product, including Dole Apple Juice (primary package), 15.2 Fl oz., PET, 12 bottles per case, Refrigerate after opening.

Why was it recalled?

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

What does Class II mean?

FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.

Where was it sold or shipped?

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

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

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Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.