CLASS II Food recall · Reported 4 Apr 2018 · FDA Enforcement Report

Sour Patch Kids recalled by Mondelez Global

Mondelez Global is recalling Sour Patch Kids, distributed in 12 states. The recall was initiated on 13 Mar 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesRetail UPC; Number of Retail Units 0 70462 43309 8; / 1 Retail Unit Case UPC; Units Per Case 0 00 70462 00043 6; / 4 Units per Case
Quantity recalled1814 Cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0952-2018
FDA event ID
79546
Recalling firm
Mondelez Global, East Hanover, NJ
Classification
Class II
Status
Terminated
Recall initiated
13 Mar 2018
FDA classified
23 Mar 2018
Reported
4 Apr 2018
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Peanuts
Product category
Other

Timeline

13 Mar 2018Recall initiated by company
23 Mar 2018Classified by FDA+10 days
4 Apr 2018Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Mondelez Global LLC is initiating a recall because remnants of a half peanut shell were found in two containers of bulk candy from a single lot during the repacking process and the candy is not labeled as containing peanuts. Mondelez Global LLC after an investigation, including inspection of product within in their control from the same lot did not find any other evidence of peanut contamination. The firm believes this is most likely to be an isolated incident and that product on the market is unlikely to contain any peanut pieces and the product is not likely to cause adverse health consequences to peanut allergic consumers. No adverse health events have been reported. Never the less, out of an abundance of caution, we have determined to conduct a voluntary recall to the retail level.

Product as listed by the FDA

Sour Patch Kids, 1.9 lb bag

Where it was distributed

The product has been distributed to the following States: AZ, CA, CT, GA, IL, KY, ME, NC, NJ, NY, Ok, PA, VA

ArizonaCaliforniaConnecticutGeorgiaIllinoisKentuckyMaineNorth CarolinaNew JerseyNew YorkPennsylvaniaVirginia

Questions about this recall

Is Sour Patch Kids recalled?

Yes. Mondelez Global recalled Sour Patch Kids on 13 Mar 2018. The recall is Class II and its status is Terminated. Recall number F-0952-2018.

Why was it recalled?

Mondelez Global LLC is initiating a recall because remnants of a half peanut shell were found in two containers of bulk candy from a single lot during the repacking process and the candy is not labeled as containing peanuts. Mondelez Global LLC after an investigation, including inspection of product within in their control from the same lot did not find any other evidence of peanut contamination. The firm believes this is most likely to be an isolated incident and that product on the market is unlikely to contain any peanut pieces and the product is not likely to cause adverse health consequences to peanut allergic consumers. No adverse health events have been reported. Never the less, out of an abundance of caution, we have determined to conduct a voluntary recall to the retail level.

Which lots are affected?

Retail UPC; Number of Retail Units 0 70462 43309 8; / 1 Retail Unit Case UPC; Units Per Case 0 00 70462 00043 6; / 4 Units per Case

Where was it sold?

The product has been distributed to the following States: AZ, CA, CT, GA, IL, KY, ME, NC, NJ, NY, Ok, PA, VA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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