Sweet & Spicy BBQ sauce, Fresh Chile BBQ sweet & Spicy Medium. 19 fluid ounce glass jar 19 fl oz. (510g) , with a metal
Summary
The FDA issued a Class II for Sweet & Spicy BBQ sauce, Fresh Chile BBQ sweet & Spicy Medium. 19 fluid ounce gl by The Fresh Chile Company. Reason: Label lacked Fish (anchovies) allergen declaration..
Details
Source
Food Recall
External ID
F-1700-2023
Action Date
2023-10-11
Status
Terminated
Category
food
Product Description
Sweet & Spicy BBQ sauce, Fresh Chile BBQ sweet & Spicy Medium. 19 fluid ounce glass jar 19 fl oz. (510g) , with a metal screw top lid.
Lot/Code Info: Lot #'s 062122-21 062122-31 062222-21 062222-31 062322-21 062322-31 062722-11 062722-21 062722-31 Lot code is the date of cook then dash, the kettle # and cook in that kettle on that day, as in Kettle 2 first cook (21)
Quantity Affected: 6,475 individual units distributed to wholesale customers and individuals via firms website and gift shop.
Reason for Recall
Label lacked Fish (anchovies) allergen declaration.
Distribution
6,453 6,475 19 fl oz. (510g) jars distributed to wholesale customers and individuals. From June 21 2022 last date of distribution April 12 2023. With 81 sold through the giftshop from April 13th to August 25 2023. Wholesale customers 28, internet customers to be determined. 18 6,453 6,475 19 fl oz. (510g) jars remain in the firms possession, under quarantine.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-25
Company
Las Cruces, NM
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 163 food recalls issued in the same week, part of 204 food-related FDA actions this month.
The Fresh Chile Company has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (The Fresh Chile Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The Fresh Chile Company have FDA actions?
The Fresh Chile Company has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1700-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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