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Lower risk Food recall · FDA · Published March 13, 2018

Mondelez Recalls Sour Patch Kids Bags Due to Possible Peanut Shells

Mondelez recalls Sour Patch Kids 1.9 lb bags after finding peanut shells in a small batch during repacking. The product is not labeled as containing peanuts but may pose a risk for peanut allergies.

🇺🇸 FDA recall #F-0952-2018FoodMondelez ›
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Recalling firmMondelez Global Llc100 Deforest Ave · East Hanover, NJ 07936-2813
✎ GovInfoNow plain-language explainer

What happened, in plain English

Mondelez is recalling Sour Patch Kids 1.9 lb bags because peanut shells were found in a small batch during repacking. The company says this is likely an isolated incident and the product won't cause health issues for peanut-allergic people, but they're recalling it out of caution. Read more at govinfonow.com/recall/19573-mondelez-recalls-sour-patch-kids-bags-due-to-possible-peanut.

Source Summary by GovInfoNow · govinfonow.com/recall/19573-mondelez-recalls-sour-patch-kids-bags-due-to-possible-peanut · Updated October 7, 2026 · FDA enforcement record: FDA #F-0952-2018

Cite this page

“Mondelez Recalls Sour Patch Kids Bags Due to Possible Peanut Shells.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19573-mondelez-recalls-sour-patch-kids-bags-due-to-possible-peanut. Based on FDA recall #F-0952-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0952-2018%22&limit=1).

Why it’s dangerous

Peanut shells were found in a small batch of Sour Patch Kids during repacking. The company states this is likely an isolated incident and the product is not labeled as containing peanuts, so it shouldn't cause health issues for peanut-allergic people.

Who’s affected

Peanut-allergic consumers who bought Sour Patch Kids 1.9 lb bags from retailers. The risk is low because the company says this is an isolated incident and the product is unlikely to cause health issues.

How to tell if you have this one

Check for Sour Patch Kids 1.9 lb bags with UPC 70462 43309 8 or case UPC 70462 00043 6. The product was sold in retail stores.

  • Brand
    Mondelez
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC 70462 43309 8 on the bag or case UPC 70462 00043 6 to confirm if it's affected.

Where it went and when

Where it was distributed

Distributed in 13 states.

Alaska: not listedAKMaine: yesMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: yesKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “The product has been distributed to the following States: AZ, CA, CT, GA, IL, KY, ME, NC, NJ, NY, Ok, PA, VA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Connecticut, Georgia, Illinois, Kentucky, Maine, New Jersey, New York, North Carolina, Oklahoma, Pennsylvania, Virginia.

Recall timeline

FDA terminated this recall 3.4 years after the firm started it.

1. Firm started the recall: Mar 13, 201812. FDA classified it Class II: Mar 23, 201823. Published in FDA’s Enforcement Report: Apr 4, 201834. FDA terminated the recall: Aug 17, 2021420182021
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0952-2018 (March 13, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0952-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA