Food Recall Check
Class II · Moderate risk Terminated Initiated Aug 30, 2019 (7 years ago)

Cena Vegan Pollo Asado Plant-Based Meat recall

Recalled by Cena Vegan · Los Angeles, CA, United States

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

Why it was recalled

California Department of Public Health conducted an inspection and found that hydrolyzed soy protein was not declared as a sub ingredient or allergen.

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

Cena Vegan Pollo Asado Plant-Based Meat; Net Wt. 16 oz. (448 grams) retail, Net Wt. 5 lb. - food service; UPC: 8 55687 00701 5; Ingredient: Vital wheat gluten, Garbanzo bean flour, Vegetable bouillon, Orange juice, Less than 2% of: Vegetable Oil, Lime Juice, Onion Powder, Garlic Powder, Garlic, Paprika, Cumin, Coriander. Contains: Wheat.

Quantity: 3,685 lbs.

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 dates from 04/15/20 to 9/24/20.

Where it was sold

California Florida Hawaii Missouri Washington

FDA's distribution note: CA, WA, HI,MO, FL

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
Cena Vegan
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 30, 2019
In FDA report of
Sep 18, 2019
Terminated
Jan 2, 2020
FDA recall number
F-2154-2019 · event 83723
Official record
FDA enforcement report search