RecallHawk
Class I Recall

PICO DE GALLO-MILD-4oz PICO DE GALLO-MILD-6/14oz PICO DE GALLO-4/5# PICO DE GALLO-1/5# PICO DE GALLO-MILD-1/5#

NatureBest Pre-Cut & Produce LLc

Summary

The FDA issued a Class I for PICO DE GALLO-MILD-4oz PICO DE GALLO-MILD-6/14oz PICO DE GALLO-4/5# PICO DE GALL by NatureBest Pre-Cut & Produce LLc. Reason: Jalapenos have the potential to be contaminated with Salmonella.

Details

Source

Food Recall

External ID

H-1372-2026

Action Date

2026-09-23

Status

Ongoing

Category

food

Product Description

PICO DE GALLO-MILD-4oz PICO DE GALLO-MILD-6/14oz PICO DE GALLO-4/5# PICO DE GALLO-1/5# PICO DE GALLO-MILD-1/5#

Lot/Code Info: 190A26184 - 190A26216

Quantity Affected: 62,856 cases (total)

Reason for Recall

Jalapenos have the potential to be contaminated with Salmonella

Distribution

Texas and Louisiana

Type: Voluntary: Firm initiated

Recall Initiated: 2026-08-05

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 54 food recalls issued in the same week, part of 82 food-related FDA actions this month.

NatureBest Pre-Cut & Produce LLc has 9 FDA actions in our database, including 9 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 (NatureBest Pre-Cut & Produce LLc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does NatureBest Pre-Cut & Produce LLc have FDA actions?

NatureBest Pre-Cut & Produce LLc has 9 FDA actions in our database, including 9 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1372-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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