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Alma Pak International LLC Recall: Listeria monocytogenes. During routine testing the firm received positive test results of Listeria monocytogenes on their finished product.

United States

TerminatedClass I

Company
Alma Pak International LLC
Product
FROZEN ORGANIC BLUEBERRIES, INGREDIENTS: FROZEN ORGANIC BLUE…
Recall date
June 9, 2025
Terminated
November 12, 2025
Source
FDA

Reason for recall

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

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
FROZEN ORGANIC BLUEBERRIES, INGREDIENTS: FROZEN ORGANIC BLUEBERRIES 30# Bulk Blueberries ALMA PAK INTERNATIONAL, LLC 230 Pineview Rd, Alma Ga 31510 Not published in this source record 400/30lb boxes Lot# 13325 G1060 & 13325 G 1096

Distribution

  • Product was shipped to one customer in NC and did not reach retail stores.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0204-2025
Event ID
97052
Status
Terminated
Classification
Class I
Company
Alma Pak International LLC
Product description
FROZEN ORGANIC BLUEBERRIES, INGREDIENTS: FROZEN ORGANIC BLUEBERRIES 30# Bulk Blueberries ALMA PAK INTERNATIONAL, LLC 230 Pineview Rd, Alma Ga 31510
Quantity
400/30lb boxes
Reason
Listeria monocytogenes. During routine testing the firm received positive test results of Listeria monocytogenes on their finished product.
Recall initiation date
June 9, 2025
Report date
July 9, 2025
Classification date
Not published in this source record
Termination date
November 12, 2025
Distribution pattern
Product was shipped to one customer in NC and did not reach retail stores.
UPC, lot, and code information
Lot# 13325 G1060 & 13325 G 1096
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Alma Pak International LLC

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
North Carolina 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

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