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Lower risk Food recall · FDA · Published October 28, 2016

Mondelez Recalls Oreo Fudge Creme Mint Variety Due to Missing Milk Allergen Label

Mondelez is recalling certain Oreo Fudge Cremes (Original and mint varieties) because milk allergen is not listed on the ingredient label. This poses a risk for people with milk allergies.

🇺🇸 FDA recall #F-0672-2017FoodMondelez ›
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Recalling firmMondelez International200 Deforest Ave · East Hanover, NJ 07936-2833
✎ GovInfoNow plain-language explainer

What happened, in plain English

Mondelez is recalling Oreo Fudge Creme Mint Variety (11.3 oz) because it doesn't list milk as an allergen. This could cause allergic reactions in people sensitive to milk. Read more at govinfonow.com/recall/22963-mondelez-recalls-oreo-fudge-creme-mint-variety-due-to-missing.

Source Summary by GovInfoNow · govinfonow.com/recall/22963-mondelez-recalls-oreo-fudge-creme-mint-variety-due-to-missing · Updated October 9, 2026 · FDA enforcement record: FDA #F-0672-2017

Cite this page

“Mondelez Recalls Oreo Fudge Creme Mint Variety Due to Missing Milk Allergen Label.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/22963-mondelez-recalls-oreo-fudge-creme-mint-variety-due-to-missing. Based on FDA recall #F-0672-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0672-2017%22&limit=1).

Why it’s dangerous

The product does not list milk as an allergen on the ingredient label. This means individuals with milk allergies could unknowingly consume the product and react.

Who’s affected

People with milk allergies who consume the product may experience an allergic reaction. The recall affects specific Oreo Fudge Creme varieties sold between August and October 2016.

How to tell if you have this one

Check for the product name 'Nabisco Oreo Fudge Creme Mint Variety' with a net weight of 11.3 oz. The recall covers items distributed by Mondelez Global LLC in East Hanover, NJ between August and October 2016.

  • Brand
    Mondelez
  • Product
    Nabisco Oreo Fudge Creme Mint Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    Nationwide, PR, St. Croix and St. Thomas Phillipines
Recall numberProduct, codes & lots
F-0671-2017Nabisco Oreo Fudge Creme Original Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC 044000026943; 19 AUG 16 20 Aug 16 14 SEP 16 13 OCT 16 14 OCT 16 17 OCT 16
F-0672-2017Nabisco Oreo Fudge Creme Mint Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC 044000026967; 20 AUG 16 21 AUG16 14 SEP 16 15 SEP 16 16 SEP 16 17 OCT 16 18 OCT 16
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the ingredient list to confirm milk is not listed as an allergen.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFLPuerto Rico: yesPR

FDA distribution: “Nationwide, PR, St. Croix and St. Thomas Phillipines” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 19 months after the firm started it.

1. Firm started the recall: Oct 28, 201612. FDA classified it Class I: Dec 8, 201623. Published in FDA’s Enforcement Report: Dec 14, 201634. FDA terminated the recall: May 22, 2018420162018
  1. Firm started the recall
  2. FDA classified it Class I
  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-0672-2017 (October 28, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0672-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 9, 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