Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 2, 2016 (11 years ago)

MAGGI Chicken Flavor Bouillon 6Tab recall

Recalled by Nestle USA · Glendale, CA, United States

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

Why it was recalled

Nestle USA is recalling MAGGI Chicken Bouillon tablets because of undeclared wheat.

Undeclared allergen: Wheat

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

MAGGI Chicken Flavor Bouillon 6Tab, 12Tab UPC Codes: 028000247959, 028000115678, 028000115678

Quantity: 558,325 units

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.

Production Codes: All Best Before ending in years 2015, 2016, 2017

Where it was sold

Alabama Arizona California Florida Georgia Illinois Massachusetts Maryland Maine Michigan Mississippi North Carolina New Jersey New Mexico Nevada New York Ohio Oklahoma Pennsylvania South Carolina Tennessee Texas Utah Virginia Wyoming

FDA's distribution note: U.S. distribution to the following; CA, FL, TX, IL, GA, NJ, MI, MA, PA, NY, NC, OH, MD, NM, SC, AL, TN, OK, MS, AZ, ME, VA, NV, WY, UT, AL. No foreign distribution.

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 wheat; 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
Nestle USA
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 2, 2016
In FDA report of
Apr 6, 2016
Terminated
Jun 29, 2016
FDA recall number
F-0797-2016 · event 73425
Official record
FDA enforcement report search

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