Label lacked Fish (anchovies) allergen declaration.
Health risk
The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.
Action required
Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.
Recall closed · classified by the FDAFL, INMore food
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The Fresh Chile CompanyLas Cruces, NM, United States
UPC / barcodes
No UPC listed in the FDA enforcement record.
Lot / date codes
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)
Distribution area
FLIN
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.
United States
Quantity affected
6, 475 individual units distributed to wholesale customers and individuals via firms website and gift shop.
Recall initiation
FDA report date: October 11, 2023
FDA recall number
F-1700-2023
Beyond the headline
The recall, in context
The Fresh Chile Company initiated this food recall on August 25, 2023. The FDA enforcement report states: Label lacked Fish (anchovies) allergen declaration. The FDA report lists distribution as: 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.
The FDA enforcement report describes the reason as: Label lacked Fish (anchovies) allergen declaration.
Sweet & Spicy Bbq Sauce, Fresh Chile Bbq Sweet & Spicy Medium was made or distributed by The Fresh Chile Company in Las Cruces, NM, United States. This page reflects FDA report F-1700-2023, dated October 11, 2023.
Why this is a Class II recall
Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.
FDA definition
The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.
What to do now
1
Stop using it
Do not eat, drink or take the affected product.
2
Check the codes
Compare the lot and date codes against the table above.
3
Return or discard
Contact the retailer or recalling firm about a refund, and dispose of the product safely.
Consumer safety guide
Undeclared fish
Symptoms to watch for
Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a fish allergy.
When symptoms may appear
Reactions can begin within minutes to a few hours after eating the product.
Higher-risk groups
People with a diagnosed fish allergy, especially anyone with a history of anaphylaxis.
What to do now
1Do not eat the product if you have a fish allergy.
2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
3Keep the packaging and contact the retailer or manufacturer about a refund.
This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.
Frequently asked
Questions about this recall
4 answers
What is the Sweet & Spicy Bbq Sauce, Fresh Chile Bbq Sweet & Spicy Medium recall?
The Fresh Chile Company recalled Sweet & Spicy Bbq Sauce, Fresh Chile Bbq Sweet & Spicy Medium in an FDA Class II enforcement action reported as F-1700-2023. Label lacked Fish (anchovies) allergen declaration.
What should I do if I bought this product?
Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Do not eat the product if you have a fish allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.
Is the The Fresh Chile Company recall still active?
The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.
Where can I verify this recall?
This page is normalized from the openFDA enforcement record F-1700-2023. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.
Verify before you act.
VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.