Class IITerminated in FDA datasetRecall initiated Mar 5, 2020

Stonewall Kitchen, Ghost Pepper Salsa, Net Weight 454g (16oz)

Recalling firm: Stonewall Kitchen, LLC

Why it was recalled

Product is mislabeled as salsa but it contains queso and does not declare two allergens, specifically milk and soy.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 19, 2020.

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Compare the exact product and package details with the label you have.

ProductStonewall Kitchen, Ghost Pepper Salsa, Net Weight 454g (16oz), Ingredients: Tomatoes, Jalapeno Peppers, Onion, Tomato Puree, Green Chile Peppers, Distilled Vinegar, Salt, Dehydrated Ghost Pepper, Dehydrated Garlic, Spices, Dehydrated Cilantro. UPC 7 11381 32738 8. BEST BY 23MAY2021. Packaged in 16 oz. glass jars with brushed silver lid.
Package size454g
UPC711381327388

FDA code information

UPC 7 11381 32738 8. BEST BY 23MAY2021.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Stonewall Kitchen, Ghost Pepper Salsa, Net Weight 454g (16oz), Ingredients: Tomatoes, Jalapeno Peppers, Onion, Tomato Puree, Green Chile Peppers, Distilled Vinegar, Salt, Dehydrated Ghost Pepper, Dehydrated Garlic, Spices, Dehydrated Cilantro. UPC 7 11381 32738 8. BEST BY 23MAY2021. Packaged in 16 oz. glass jars with brushed silver lid.

Extracted codes and context

TypeCode / valueContext
UPC711381327388UPC 7 11381 32738 8. BEST BY 23MAY2021.
UPC711381327388t, Dehydrated Ghost Pepper, Dehydrated Garlic, Spices, Dehydrated Cilantro. UPC 7 11381 32738 8. BEST BY 23MAY2021. Packaged in 16 oz. glass jars with brushed silver lid.

Original FDA recall reason

Product is mislabeled as salsa but it contains queso and does not declare two allergens, specifically milk and soy.

Recall details

Recall number
F-0835-2020
Event ID
85156
FDA status
Terminated
Initiated
Mar 5, 2020
Reported
Mar 18, 2020
Classified
Mar 16, 2020
Terminated
May 19, 2020
Quantity
4,800 units
Location
York, ME, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KY, MA, MD, ME, MI, MN, MO, MT, NC, ND, NH, NJ, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI, WV, WY

FDA source record · F-0835-2020

Data updated September 16, 2026. View official FDA data ↗

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