CLASS II ONGOING Food recall · Reported 16 Sep 2026 · FDA Enforcement Report
Fannie May & XO Marshmallow Pixie S'mores Collection recalled
Ferrero USA is recalling Fannie May & XO Marshmallow Pixie S'mores Collection, distributed in Iowa, Illinois, Indiana, Ohio. The recall was initiated on 14 Aug 2026 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-1334-2026
- FDA event ID
- 99682
- Recalling firm
- Ferrero USA, North Canton, OH
- Brand
- Fannie May
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 14 Aug 2026
- FDA classified
- 9 Sep 2026
- Reported
- 16 Sep 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Tree Nuts
- Product category
- Candy
Timeline
| 14 Aug 2026 | Recall initiated by company | |
| 9 Sep 2026 | Classified by FDA | +26 days |
| 16 Sep 2026 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared milk and pecans
Product as listed by the FDA
Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz
Where it was distributed
IA, IL, IN, OH
Questions about this recall
Is Fannie May & XO Marshmallow Pixie S'mores Collection recalled?
Yes. Ferrero USA recalled Fannie May & XO Marshmallow Pixie S'mores Collection on 14 Aug 2026. The recall is Class II and its status is Ongoing. Recall number H-1334-2026.
Why was it recalled?
Undeclared milk and pecans
Which lots are affected?
All best by codes that were sold 8/7/2026 to 8/14/2026
Where was it sold?
IA, IL, IN, OH
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 22 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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