RecallHawk
Class I Recall

FRESH CREATIVE FOODS COOKED PENNE PASTA 8 x 3 lb pouches Net Weight: 24 lbs (10.88 kg) PERISHABLE KEEP REFRIGERATED

Nate's Fine Foods, LLC

Summary

The FDA issued a Class I for FRESH CREATIVE FOODS COOKED PENNE PASTA 8 x 3 lb pouches Net Weight: 24 lbs (10. by Nate's Fine Foods, LLC. Reason: Potential contamination with Listeria monocytogenes..

Details

Source

Food Recall

External ID

H-0077-2026

Action Date

2025-10-15

Status

Ongoing

Category

food

Product Description

FRESH CREATIVE FOODS COOKED PENNE PASTA 8 x 3 lb pouches Net Weight: 24 lbs (10.88 kg) PERISHABLE KEEP REFRIGERATED

Lot/Code Info: Lot: 2382521, 2452521, 2572524, 2512523 USE BY: 10/10/2025, 10/17/2025, 10/23/2025, 10/29/2025

Quantity Affected: 1,337 cases (32,088 lbs)

Reason for Recall

Potential contamination with Listeria monocytogenes.

Distribution

CA, IN, PA, TX

Type: Voluntary: Firm initiated

Recall Initiated: 2025-09-25

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Nate's Fine Foods, LLC has 10 FDA actions in our database, including 10 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Nate's Fine Foods, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Nate's Fine Foods, LLC have FDA actions?

Nate's Fine Foods, LLC has 10 FDA actions in our database, including 10 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0077-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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