Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 1, 2021 (5 years ago)

Adobo para Chorizo recall

Recalled by Jesmar Spices, LLC · Portland, OR, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Undeclared SOY LECITHIN. The firm used chocolate bar in their Adobo para Chorizo Seasoning for Sausage and does not declare the chocolate bar's sub-ingredient soy lecithin in finished product label.

Undeclared allergen: Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Adobo para Chorizo - Chorizo Marinade - Seasoning for Sausage. Product is packaged in a plastic bucket seal with lid, 5 gallons. No UPC. The label is read in parts: "*** Adobo para Chorizo *** Seasoning for Sausage *** Ingredients: Dried Chilies, vinegar, almonds, salt, pepper, garlic, cumin, clove, oregano, mint, cinnamon, saffron, cocoa, bay leaves, artificial food coloring (red and yellow)*** Jesmar Spices ***Portland, OR ***".

Quantity: 2 containers

Food: Spices & seasonings

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Expiration date on 6/27/21

Where it was sold

Oregon

FDA's distribution note: distributed in OR.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Jesmar Spices, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 1, 2021
In FDA report of
Jun 16, 2021
Terminated
Jun 9, 2021
FDA recall number
F-0663-2021 · event 88039
Official record
FDA enforcement report search

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