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Use caution Food recall · FDA · Published May 13, 2026

Nutrisystem Chocolate Cheesecake Recall: Undeclared Soy Allergen

Nutrisystem is recalling 2 oz Chocolate Cheesecake packages due to undeclared soy. Check your lot code CH030426 and product code 40007.

🇺🇸 FDA recall #H-0947-2026FoodNutrisystem ›
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Recalling firmNutrisystem Inc600 Office Center Dr · Fort Washington, PA 19034-3232
✎ GovInfoNow plain-language explainer

What happened, in plain English

Nutrisystem Inc. has recalled specific packages of its Chocolate Cheesecake because the product contains undeclared soy, which is not listed on the label. This poses a risk to individuals with soy allergies who may consume the product unknowingly. The recall covers 5,184 units distributed across several states. Read more at govinfonow.com/recall/6225-nutrisystem-chocolate-cheesecake-recall-undeclared-soy-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/6225-nutrisystem-chocolate-cheesecake-recall-undeclared-soy-allergen · Updated October 9, 2026 · Official notice: FDA #H-0947-2026

Cite this page

“Nutrisystem Chocolate Cheesecake Recall: Undeclared Soy Allergen.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/6225-nutrisystem-chocolate-cheesecake-recall-undeclared-soy-allergen. Based on FDA recall #H-0947-2026.

Why it’s dangerous

The hazard is an undeclared allergen, meaning soy is present in the food but not disclosed on the packaging. For people with severe soy allergies, ingesting even a small amount can trigger a serious allergic reaction.

Who’s affected

Consumers who purchased Nutrisystem Chocolate Cheesecake in the affected states and have a soy allergy are at risk of an allergic reaction. Anyone who bought the specific lot code CH030426 should check their product.

How to tell if you have this one

Look for Nutrisystem Chocolate Cheesecake packages that are 2 oz (57g), flow-wrapped, and kept frozen. You must check the product code 40007 and lot code CH030426 to confirm if your item is part of this recall.

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

What to do — step by step

  1. Check Your Product Codes

    Verify that your package has product code 40007 and lot code CH030426.

  2. Avoid Consumption

    Do not eat the recalled Chocolate Cheesecake if you have a soy allergy or if the codes match.

Where it went and when

Where it was distributed

Distributed in 26 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “The recalled product was distributed to the following states: AL, AR, CO,GA, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, ND, NE, NM, OH, OK, SC, SD, TN, TX, WI, WV, WY” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Arkansas, Colorado, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New Mexico, North Dakota, Ohio, Oklahoma, South Carolina, South Dakota, Tennessee, Texas, West Virginia, Wisconsin, Wyoming.

Recall timeline

FDA published this recall 42 days after the firm started it.

1. Firm started the recall: May 13, 202612. FDA classified it Class II: Jun 16, 202623. Published in FDA’s Enforcement Report: Jun 24, 202632026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

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 #H-0947-2026 (May 13, 2026)
  • Plain-language summary written by qwen3.6:35b-a3b 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