La Reyna Salsa Verde, Gluten Free / Medium. Product Code 1784. Net Wt 16 oz. UPC 7 52830-92640 0. Ingredients: Toma
Summary
The FDA issued a Class III for La Reyna Salsa Verde, Gluten Free / Medium. Product Code 1784. Net Wt 16 oz. by Twin Cities Co-Op Partners Inc.. Reason: Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers..
Details
Source
Food Recall
External ID
F-1497-2023
Action Date
2023-09-20
Status
Terminated
Category
food
Product Description
La Reyna Salsa Verde, Gluten Free / Medium. Product Code 1784. Net Wt 16 oz. UPC 7 52830-92640 0. Ingredients: Tomatillo, Jalapenos, Onions, Garlic, Salt. Keep Refrigerated. La Reyna, 202 4th, Vinton IA 42349
Lot/Code Info: Best By: 8/18/2023
Quantity Affected: 720 containers total
Reason for Recall
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Distribution
IA, MI, MN, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-11
Company
Saint Paul, MN
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Twin Cities Co-Op Partners Inc. has 5 FDA actions in our database, including 5 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (Twin Cities Co-Op Partners Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Twin Cities Co-Op Partners Inc. have FDA actions?
Twin Cities Co-Op Partners 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-1497-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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