FDA recall record

Country Favor Best Taste Brand Salted Shrimp Paste Sauce recall — FDA H-0009-2025

Product contains undeclared FD&C Red #3

Class IIIclassification
H-0009-2025official record ID
Jun 11, 2025report date

Recall record at a glance

Official recordH-0009-2025
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmCountry Favor Inc.
Report dateJun 11, 2025
Recall initiation dateMay 20, 2025
QuantityN/A
LocationMaspeth, NY, United States

Official product description

Best Taste Brand Salted Shrimp Paste Sauce; ING: Shrimp, sugar, salt; COUNTRY FAVOR, INC; PRODUCT OF VIETNAM; Net Weight: 12 oz (350 g)

Why the product was recalled

Product contains undeclared FD&C Red #3

Distribution information

CT, GA, IL, IN KS, KY, LA, MA, MN, MO, MS, NC, OH, OK, PA, TN, TX, VA, NY

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.