RecallHawk
Class I Recall

Guacamole & Pico de Gallo Combo $7.99 - 16 oz 639123880574 Guacamole Chunky Medium - 14 oz 639123880161 Guacamol

JFE FRANCHISING INC

Summary

The FDA issued a Class I for Guacamole & Pico de Gallo Combo $7.99 - 16 oz 639123880574 Guacamole Chunky by JFE FRANCHISING INC. Reason: Listeria monocytogenes.

Details

Source

Food Recall

External ID

F-1764-2024

Action Date

2024-09-11

Status

Ongoing

Category

food

Product Description

Guacamole & Pico de Gallo Combo $7.99 - 16 oz 639123880574 Guacamole Chunky Medium - 14 oz 639123880161 Guacamole Chunky Mild - 14 oz 639123880154 Guacamole Blender Mild $5.99 - 12 oz 639123880789 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 0 food recalls issued in the same week, part of 0 food-related FDA actions this month.

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 0 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1764-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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