RecallHawk
Class I Recall

Pico de Gallo Classic Hot - 14 oz 639123880116 Pico de Gallo Classic Medium - 14 oz 639123880093 Pico de Gallo C

JFE FRANCHISING INC

Summary

The FDA issued a Class I for Pico de Gallo Classic Hot - 14 oz 639123880116 Pico de Gallo Classic Medium by JFE FRANCHISING INC. Reason: Listeria monocytogenes.

Details

Source

Food Recall

External ID

F-1762-2024

Action Date

2024-09-11

Status

Ongoing

Category

food

Product Description

Pico de Gallo Classic Hot - 14 oz 639123880116 Pico de Gallo Classic Medium - 14 oz 639123880093 Pico de Gallo Classic Mild - 14 oz 639123880109 Plastic Clam-Shell Container

Lot/Code Info: Sell by 7/9/24 THROUGH Sell by 7/26/24

Reason for Recall

Listeria monocytogenes

Distribution

KY MI OH WV

Type: Voluntary: Firm initiated

Recall Initiated: 2024-07-19

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

JFE FRANCHISING INC has 20 FDA actions in our database, including 20 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 (JFE FRANCHISING INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does JFE FRANCHISING INC have FDA actions?

JFE FRANCHISING INC has 20 FDA actions in our database, including 20 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1762-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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