CLASS II Food recall · Reported 22 Oct 2025 · FDA Enforcement Report

Dole Apple Juice (primary package), PET, Refrigerate after opening recalled

Tropicana Brands Group is recalling Dole Apple Juice (primary package), PET, Refrigerate after opening, distributed in 11 states. The recall was initiated on 11 Sep 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesCase 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 recalled1,599 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0073-2026
FDA event ID
97678
Recalling firm
Tropicana Brands Group, Chicago, IL
Brand
Dole
Classification
Class II
Status
Terminated
Recall initiated
11 Sep 2025
FDA classified
16 Oct 2025
Reported
22 Oct 2025
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Mold
Product category
Juice

Timeline

11 Sep 2025Recall initiated by company
16 Oct 2025Classified by FDA+35 days
22 Oct 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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

Where it was distributed

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

ArkansasColoradoIowaKansasMissouriMississippiNebraskaNew MexicoOklahomaTennesseeTexas

Questions about this recall

Why was it recalled?

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

Which lots are affected?

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 was it sold?

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 it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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