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Mondelez
Recall · Class II2014-08-27Terminated

Contains soy without saying so on the label, which matters if you are allergic to it.

Mondelez Global LLC is conducting a voluntary recall of Chiclets Chewing Gum due to undeclared soy lecithin on the label.

Above, in the agency’s own words. The line before it is our plain-English summary — how we word these.

Issued by the US Food and Drug Administration, naming Mondelez.

What the notice covered

1) Chiclets Peppermint Gum, 6-10 piece packages (60 pieces), Retail UPC 0 12546 10105 9; 2)Chiclets Peppermint Gum, 20 - 12 piece packages (240 pieces), Retail UPC 0 12546 02501 0, Case UPC 1001254 3)Chiclets Peppermint Gum, (12 pieces), Retail UPC 0 12546 10128 8; 4)Chiclets Peppermint Gum, 7-6 PAK packages (420 pieces), Retail UPC 0 12546 02601 7, Case UPC 000125461010

Quoted from the record as published. If a product is not described here, this notice does not tell us whether it was affected.

What Class II means

The FDA’s middle class: use of the product may cause temporary or medically reversible health consequences, and the probability of serious harm is remote.

This is the agency’s own definition of the class. We do not assign classes and we do not rank them against each other.

The record

Agency
US Food and Drug Administration (FDA)
Reference number
F-0500-2015
Kind of action
Recall
Dated
2014-08-27
Terminated
2017-02-13
Status on the record
Terminated
We read it
2026-10-01

Regulates most packaged food, drugs and devices. Its recall records are published weekly in the Enforcement Report.

Products we matched to this notice

Chiclets, Peppermint Gumthe notice printed this product’s barcode: “0 12546 10105 9”
Chiclets, Original Candy Coated Gum, Peppermintthe notice printed this product’s barcode: “0 12546 02601 7”

How we are treating it

This notice concerns the product line itself or how it was produced.

The government record

The FDA publishes this notice through its enforcement API, so the link below returns raw JSON rather than a readable page. It is the primary record and we cite it as such; everything above is our transcription of it.

https://api.fda.gov/food/enforcement.json?search=recall_number:"F-0500-2015"

To see it in the FDA’s own words, search the reference number F-0500-2015 in the Search the FDA Enforcement Report. The FDA publishes no direct link to an individual recall.

How we source every record on this site