Check the Batch
Class IITerminated in FDA datasetAug 27, 2014

1) Chiclets Peppermint Gum, 6-10 piece packages (60 pieces), 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.

Check the codes ↓

The exact product

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

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

1)Best When Used By 12 Oct 2015 - 6 Nov 2015; 2)Best When Used By 31 Aug 2014 - 8 Nov 2015; 3)Best When Used By 31 Aug 2014 - 8 Nov 2015; 4)Best When Used By 12 Oct 2015 - 6 Nov 2015

TypeCode / valueContext
UPC0125460250105 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 PA
UPC0125460260176 10128 8; 4)Chiclets Peppermint Gum, 7-6 PAK packages (420 pieces), Retail UPC 0 12546 02601 7, Case UPC 000125461010
UPC0125461010591) 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)Chiclet
UPC01254610128846 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

Recall details

Recall number
F-0500-2015
Event ID
69335
FDA status
Terminated
Initiated
Aug 27, 2014
Reported
Nov 19, 2014
Classified
Nov 13, 2014
Terminated
Feb 13, 2017
Quantity
approx. 1,993,432 units
Location
East Hanover, NJ, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

US Nationwide

FDA source record · F-0500-2015

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

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.