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