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Lower risk Food recall · FDA · Published March 12, 2026

Lidl recalls Favorina Chocolate Ladybugs Nougat due to unlabeled tree nuts

Lidl US recalls Favorina Chocolate Ladybugs German-Style Nougat (UPC 2030 4492) because tree nut type isn't specified on label. Consumers with nut allergies should avoid this product.

🇺🇸 FDA recall #H-0631-2026FoodLidl ›
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Recalling firmLidl US TRADING3500 S Clark Pl · Arlington, VA 22202
✎ GovInfoNow plain-language explainer

What happened, in plain English

Lidl is recalling Favorina Chocolate Ladybugs German-Style Nougat due to the label not specifying which tree nut is present. This poses a risk for people with tree nut allergies who may be allergic to the unlisted nut type. Read more at govinfonow.com/recall/6656-lidl-recalls-favorina-chocolate-ladybugs-nougat-due-to-unlabeled-tree.

Source Summary by GovInfoNow · govinfonow.com/recall/6656-lidl-recalls-favorina-chocolate-ladybugs-nougat-due-to-unlabeled-tree · Updated August 17, 2026 · Official notice: FDA #H-0631-2026

Cite this page

“Lidl recalls Favorina Chocolate Ladybugs Nougat due to unlabeled tree nuts.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6656-lidl-recalls-favorina-chocolate-ladybugs-nougat-due-to-unlabeled-tree. Based on FDA recall #H-0631-2026.

Why it’s dangerous

The product contains tree nuts but the label does not specify which type. This could cause allergic reactions in individuals sensitive to the unlisted tree nut.

Who’s affected

People with tree nut allergies are at risk if they consume this product. The recall affects consumers who bought the product from Lidl stores or online.

How to tell if you have this one

Check for the product name 'Favorina Chocolate Ladybugs German-Style Nougat' with UPC 2030 4492. The product was distributed by Lidl US, LLC and sold in the US.

  • Brand
    Lidl
  • Product
    Favorina Chocolate Ladybugs German-Style Nougat, Net Wt 3.52 oz (100g). UPC 2030 4492. Distributed By Lidl US, LLC
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Label

    Look for the product name and UPC 2030 4492 on the package.

Where it went and when

Where it was distributed

Distributed in 9 states and D.C..

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: 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: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “DC, DE, GA, MD, NC, NJ, NY, PA, SC, VA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Delaware, District of Columbia, Georgia, Maryland, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, Virginia.

Recall timeline

FDA published this recall 20 days after the firm started it.

1. Firm started the recall: Mar 12, 202612. FDA classified it Class II: Mar 25, 202623. Published in FDA’s Enforcement Report: Apr 1, 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-0631-2026 (March 12, 2026)
  • Plain-language summary written by qwen3:4b on August 17, 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