Class ITerminatedVoluntary: Firm initiated
Alma Pak International LLC: food recall H-0204-2025
Alma Pak International LLC of Alma, GA recalled FROZEN ORGANIC BLUEBERRIES, INGREDIENTS: FROZEN ORGANIC BLUEBERRIES 30# Bulk Blueberries ALMA PAK INTERNATIONAL, LLC… Reason: Listeria monocytogenes. During routine testing the firm received positive test results of Listeria monocytogenes on their finished product. The FDA listed it as Class I in its Enforcement Report dated Jul 9, 2025; distribution: North Carolina.
Record status as published: Terminated (terminated Nov 12, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- FROZEN ORGANIC BLUEBERRIES, INGREDIENTS: FROZEN ORGANIC BLUEBERRIES 30# Bulk Blueberries ALMA PAK INTERNATIONAL, LLC 230 Pineview Rd, Alma Ga 31510
- Product quantity
- 400/30lb boxes
- Reason for recall
- Listeria monocytogenes. During routine testing the firm received positive test results of Listeria monocytogenes on their finished product.
- Codes, lots and dates on the package
- Lot# 13325 G1060 & 13325 G 1096
- Distribution pattern
- Product was shipped to one customer in NC and did not reach retail stores.
- Recalling firm
- Alma Pak International LLC, Alma, GA
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Telephone
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jun 9, 2025 |
| Classified by the FDA | Jul 1, 2025 |
| Published in the Enforcement Report | Jul 9, 2025 |
| Terminated | Nov 12, 2025 |
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0204-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.