ZANESVILLE, Ohio – Jose Madrid Salsa, a local Ohio company, has issued a voluntary recall of its Chipotle Con Queso Salsa due to undeclared Yellow 5 and Yellow 6 on the product’s ingredient label. The recall was announced on December 20, 2024, following a routine inspection by the Ohio Department of Agriculture in coordination with the U.S. Food and Drug Administration (FDA).
The affected product, packaged in 13-ounce glass jars, poses a risk for individuals with allergies or sensitivities to Yellow 5 or Yellow 6. Consumers with such allergies could experience reactions ranging from minor symptoms to potentially life-threatening conditions.
Details of the Recall
- Product Name: Chipotle Con Queso Salsa
- Brand: Jose Madrid
- UPC: 093662452935
- Lot Codes:
- 6012201 102327
- 6012201 103027
- 6012201 111227
- Packaging: Glass jars, Net Weight 13 oz.
The recalled products were sold at several holiday events in New York and North Carolina, including:
- Christmas in the Country – Hamburg, NY (Nov. 7-10, 2024)
- Syracuse Holiday Shoppes – Syracuse, NY (Nov. 8-10, 2024)
- Greensboro Holiday Market – Greensboro, NC (Nov. 15-17, 2024)
No illnesses have been reported as of the announcement date. The issue was attributed to a temporary breakdown in production and packaging processes.
What to Do If You Have the Product
Consumers who purchased the affected salsa and are allergic or sensitive to Yellow 5 or Yellow 6 are advised not to consume it. The company encourages customers to contact Jose Madrid Salsa for more information or to arrange for a return or refund.
- Contact Information:
- Phone: 740-521-4304
- Email: [email protected]
- Hours: Monday–Friday, 9 AM–5 PM
Local Response
Jose Madrid Salsa, well-known for its handcrafted products, has apologized to its customers and pledged to take corrective action to prevent similar issues in the future. The company emphasizes that the recall is precautionary and reflects its commitment to consumer safety.
Local food safety advocates remind consumers to check product labels carefully and to report any adverse reactions to their healthcare providers
