Class IITerminated in FDA datasetRecall initiated Aug 27, 2014

1) Chiclets Fruit Flavor Gum, 12 piece, Retail

Recalling firm: Mondelez Global Llc

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 13, 2017.

Check your package

Compare the exact product and package details with the label you have.

Product1) Chiclets Fruit Flavor Gum, 12 piece, Retail UPC 0 12546 10628 3; 2) Chiclets Fruit Flavor Gum, 20 - 12 piece packages (240 pieces), Retail UPC 0 12546 02503 4, Case UPC 10012
UPC012546025034, 012546106283

FDA code information

Best When Used By 30 Aug 2014 - 6 Nov 2015

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

1) Chiclets Fruit Flavor Gum, 12 piece, Retail UPC 0 12546 10628 3; 2) Chiclets Fruit Flavor Gum, 20 - 12 piece packages (240 pieces), Retail UPC 0 12546 02503 4, Case UPC 10012

Extracted codes and context

TypeCode / valueContext
UPC012546025034; 2) Chiclets Fruit Flavor Gum, 20 - 12 piece packages (240 pieces), Retail UPC 0 12546 02503 4, Case UPC 10012
UPC0125461062831) Chiclets Fruit Flavor Gum, 12 piece, Retail UPC 0 12546 10628 3; 2) Chiclets Fruit Flavor Gum, 20 - 12 piece packages (240 pieces), Retail UPC 0 12546 02503 4, Case UPC 10012

Original FDA recall reason

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

Recall details

Recall number
F-0501-2015
Event ID
69335
FDA status
Terminated
Initiated
Aug 27, 2014
Reported
Nov 19, 2014
Classified
Nov 13, 2014
Terminated
Feb 13, 2017
Quantity
1,614,000 units
Location
East Hanover, NJ, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

US Nationwide

FDA source record · F-0501-2015

Data updated September 16, 2026. View official FDA data ↗

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