Ferrero USA is recalling the Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz, because it contains undeclared milk and pecans. This poses a risk to individuals with allergies to these ingredients. The recall covers units sold between August 7, 2026, and August 14, 2026. Read more at govinfonow.com/recall/994879-fannie-may-marshmallow-pixie-recall-undeclared-milk-and-pecans.
“Fannie May Marshmallow Pixie Recall: Undeclared Milk and Pecans.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/994879-fannie-may-marshmallow-pixie-recall-undeclared-milk-and-pecans. Based on FDA recall #H-1334-2026.
The FDA announced on Aug. 14, 2026, that Ferrero USA voluntarily recalled Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz, due to undeclared milk and pecans. The recall covers products sold between Aug. 7 and Aug. 14, 2026, in Iowa, Illinois, Indiana, and Ohio.
The product contains undeclared milk and pecans, which pose a risk to consumers with allergies to these ingredients. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show other recent recalls of similar products include D'Dioses Mamey Ice Pop Recall (2026-05-04), D'Dioses Rompope Ice Pops Recall (2026-05-04), and D'Dioses Pistachio Ice Pop Recall (2026-05-04).
How to tell if you have this one
Look for the Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz package. Check the best by code on the packaging to see if it falls within the range sold from August 7, 2026, to August 14, 2026.
Brand
Fannie May & XO
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop consuming the product
Do not eat the recalled Fannie May & XO Marshmallow Pixie S'mores Collection due to undeclared allergens.
Check the best by code
Verify if your product's best by code is within the affected range of August 7, 2026, to August 14, 2026.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “IA, IL, IN, OH” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois, Indiana, Iowa, Ohio.
Recall timeline
FDA published this recall 33 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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-1334-2026 (August 14, 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.