Lunds & Byerlys Pico de Gallo / Guacamole Dip, Net Wt 18 oz (510g). UPC 0 72431-02993 6. Keep Refrigerated.
Summary
The FDA issued a Class I for Lunds & Byerlys Pico de Gallo / Guacamole Dip, Net Wt 18 oz (510g). UPC 0 72431 by Metro Produce Distributors, Inc.. Reason: Guacamole products may be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-1735-2024
Action Date
2024-08-21
Status
Terminated
Category
food
Product Description
Lunds & Byerlys Pico de Gallo / Guacamole Dip, Net Wt 18 oz (510g). UPC 0 72431-02993 6. Keep Refrigerated.
Lot/Code Info: Use By: 02-AUG-24
Quantity Affected: 66 units
Reason for Recall
Guacamole products may be contaminated with Listeria monocytogenes.
Distribution
MN
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-31
Company
Minneapolis, MN
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 125 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Metro Produce Distributors, Inc. has 5 FDA actions in our database, including 5 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 (Metro Produce Distributors, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Metro Produce Distributors, Inc. have FDA actions?
Metro Produce Distributors, Inc. has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1735-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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