Anderson's Pumpkin Pie Ice Cream May Contain Undeclared Peanuts
Anderson's Frozen Custard recalls pumpkin pie ice cream pies due to potential undeclared peanuts. Consumers should check packaging for the 9-inch clear plastic dome container.
Lower-risk recall
The Pumpkin Ice Cream Pies may contain undeclared peanuts.
Contact the company
What happened, in plain English
Anderson's Frozen Custard is recalling pumpkin pie ice cream pies that may contain undeclared peanuts. This poses a risk for people with peanut allergies who could experience an allergic reaction. Read more at govinfonow.com/recall/22798-anderson-s-pumpkin-pie-ice-cream-may-contain-undeclared-peanuts.
Source Summary by GovInfoNow · govinfonow.com/recall/22798-anderson-s-pumpkin-pie-ice-cream-may-contain-undeclared-peanuts · Updated October 8, 2026 · FDA enforcement record: FDA #F-1229-2017
Cite this page
“Anderson's Pumpkin Pie Ice Cream May Contain Undeclared Peanuts.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22798-anderson-s-pumpkin-pie-ice-cream-may-contain-undeclared-peanuts. Based on FDA recall #F-1229-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1229-2017%22&limit=1).
Why it’s dangerous
The recalled pumpkin pie ice cream pies may contain undeclared peanuts. This can trigger severe allergic reactions in individuals with peanut allergies. The hazard is specific to the product's ingredient composition.
Who’s affected
People with peanut allergies are at risk of an allergic reaction if they consume the recalled pumpkin pie ice cream pies. The product is sold seasonally from September to November.
How to tell if you have this one
Look for the 9-inch round clear plastic dome container packaging. The product is sold seasonally from September to November.
- Brand
Anderson's Frozen Custard- Category
Food
What to do — step by step
Check Packaging
Inspect the product for the 9-inch clear plastic dome container packaging.
Where it went and when
Where it was distributed
Distributed in New York.
FDA distribution: “New York” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New York.
Recall timeline
FDA terminated this recall 50 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- FDA terminated the recall
- 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 #F-1229-2017 (November 23, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1229-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.