RecallHawk
Class I Recall

Good & Gather Mexican Street Corn Trail Mix 8 oz bag UPC 085239270240, 8 bags per case

JOHN B SANFILIPPO & SONS INC

Summary

The FDA issued a Class I for Good & Gather Mexican Street Corn Trail Mix 8 oz bag UPC 085239270240, 8 bags pe by JOHN B SANFILIPPO & SONS INC. Reason: potential presence of Salmonella.

Details

Source

Food Recall

External ID

H-0835-2026

Action Date

2026-05-27

Status

Ongoing

Category

food

Product Description

Good & Gather Mexican Street Corn Trail Mix 8 oz bag UPC 085239270240, 8 bags per case

Lot/Code Info: BEST BY 23/MAR/2027 GY

Quantity Affected: 272 cases

Reason for Recall

potential presence of Salmonella

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2026-05-05

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 80 food recalls issued in the same week, part of 204 food-related FDA actions this month.

JOHN B SANFILIPPO & SONS INC has 6 FDA actions in our database, including 6 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 (JOHN B SANFILIPPO & SONS INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does JOHN B SANFILIPPO & SONS INC have FDA actions?

JOHN B SANFILIPPO & SONS INC has 6 FDA actions in our database, including 6 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0835-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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