FDA recall record

Goya Foods Pork & Beef recall — FDA F-0098-2016

Goya was notified by one of its ingredient suppliers that one lot of cumin had potentially been produced with undeclared peanut protein.

Class IIclassification
F-0098-2016official record ID
Nov 4, 2015report date

Recall record at a glance

Official recordF-0098-2016
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmGoya Foods
Report dateNov 4, 2015
Recall initiation dateFeb 13, 2015
Quantity12 fl oz - 2,372 cases (24 units/case); 24.5 fl oz - 39,070 cases (12 units/case) and 1 Gallon - 7,329 cases (6 units/case)
LocationJersey City, NJ, United States

Official product description

Goya Mojo Criollo Marinade for Chicken, Pork & Beef (a) 12 ounce (b) 24.5 oz and (c) 1 Gallon containers; Goya Foods, Inc., Secaucus, NJ 07096 USA Distributor. Product of Dominican Republic

Why the product was recalled

Goya was notified by one of its ingredient suppliers that one lot of cumin had potentially been produced with undeclared peanut protein.

Distribution information

CA, CT, DE, FL, GA, IL, IN, KY, LA, MA, MD, ME, MO, MI, MN, NC, NH, NJ, NY, OH, PA, RI, SC, TX, VA, VT, WI

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

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.

Related recall records

Other records from the same recalling company are shown first when available.