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FDA · FoodClass I

Alma Pak International LLC food recall: Frozen Organic Blueberries

Listeria

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
97052
Recall initiated
Jun 9, 2025
Classified by FDA
Jul 1, 2025
Posted in Enforcement Report
Jul 9, 2025
Terminated
Nov 12, 2025
Recalling firm
Alma Pak International LLC
Firm location
Alma, GA, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Telephone
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Listeria monocytogenes. During routine testing the firm received positive test results of Listeria monocytogenes on their finished product.

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Jun 9, 2025. FDA classified it 22 days later, on Jul 1, 2025. Distribution reported by FDA: Product was shipped to one customer in NC and did not reach retail stores.

Recalled products (1)

  • H-0204-2025 Class I Terminated

    FROZEN ORGANIC BLUEBERRIES, INGREDIENTS: FROZEN ORGANIC BLUEBERRIES 30# Bulk Blueberries ALMA PAK INTERNATIONAL, LLC 230 Pineview Rd, Alma Ga 31510

    Codes / lots: Lot# 13325 G1060 & 13325 G 1096

    Quantity: 400/30lb boxes

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 97052
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.