RecallHawk
Class II Recall

RICED CAULIFLOWER IQF NET WEIGHT: 30lbs (13.60 kg) PACK DATE: 08/04/2025 BEST BY: 08/04/2026 INGREDIENTS: CAULIFLOWER PE

Nate's Fine Foods, LLC

Summary

The FDA issued a Class II for RICED CAULIFLOWER IQF NET WEIGHT: 30lbs (13.60 kg) PACK DATE: 08/04/2025 BEST BY by Nate's Fine Foods, LLC. Reason: Potential contamination with Listeria monocytogenes..

Details

Source

Food Recall

External ID

H-0142-2026

Action Date

2025-11-05

Status

Ongoing

Category

food

Product Description

RICED CAULIFLOWER IQF NET WEIGHT: 30lbs (13.60 kg) PACK DATE: 08/04/2025 BEST BY: 08/04/2026 INGREDIENTS: CAULIFLOWER PERISHABLE KEEP FROZEN

Lot/Code Info: Lot: 2162581

Quantity Affected: 336 cases (10,080 lbs)

Reason for Recall

Potential contamination with Listeria monocytogenes.

Distribution

TX, IN

Type: Voluntary: Firm initiated

Recall Initiated: 2025-10-06

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 62 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 II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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-0142-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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