The Fresh Chile Company Recall: Label lacked Fish (anchovies) allergen declaration.

🇺🇸 United States

1. August 25, 2023 - Recall initiated
2. October 11, 2023 - Reported by source
3. August 22, 2025 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1701-2023

Event ID

92949

Status

Terminated

Classification

Class II

Company

The Fresh Chile Company

Product description

Sweet & Spicy BBQ sauce, Fresh Chile BBQ sweet & Spicy Hot. 16 fluid ounce glass jar 19 fl oz. (510g) , with a metal screw top lid.

Quantity

4,923

Reason

Label lacked Fish (anchovies) allergen declaration.

Recall initiation date

August 25, 2023

Report date

October 11, 2023

Classification date

Not published in this source record

Termination date

August 22, 2025

Distribution pattern

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.

UPC, lot, and code information

Lot #'s Lot # 091522-11 806 jars Lot # 091522-21 810 jars Lot # 110822-11 1641 jars Lot# 052923-11 1666 jars 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)

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 92949 with 1 other product entry in Public Health Trace.

Responsible company: The Fresh Chile Company

Other recalls from The Fresh Chile Company

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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