Graeter's Gluten-Free Key Lime Pie Ice Cream Recall: Contains Wheat
Graeter's Limited Edition Key Lime Pie Ice Cream is recalled for containing wheat despite being labeled gluten-free. This poses a risk for people with celiac disease or gluten allergies. Consumers should check packaging for the product code and contact Graeter's for details.
Lower-risk recall
Product is labeled as gluten free, however, it contains wheat.
Contact the company
What happened, in plain English
Graeter's Limited Edition Key Lime Pie Ice: Cream is recalled because it contains wheat, making it unsafe for people with celiac disease or gluten allergies. The product was labeled as gluten-free but was found to have wheat in its ingredients. Read more at govinfonow.com/recall/18757-graeter-s-gluten-free-key-lime-pie-ice-cream-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/18757-graeter-s-gluten-free-key-lime-pie-ice-cream-recall · Updated October 6, 2026 · FDA enforcement record: FDA #F-1837-2018
Cite this page
“Graeter's Gluten-Free Key Lime Pie Ice Cream Recall: Contains Wheat.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18757-graeter-s-gluten-free-key-lime-pie-ice-cream-recall. Based on FDA recall #F-1837-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1837-2018%22&limit=1).
Why it’s dangerous
The ice cream contains wheat, which can cause serious health issues for individuals with celiac disease or gluten allergies. Despite being labeled gluten-free, the product includes wheat in its ingredients, making it unsafe for those with these conditions.
Who’s affected
People with celiac disease or gluten allergies are at risk from this product. The recall affects consumers who purchased the limited edition Key Lime Pie Ice Cream in the U.S.
How to tell if you have this one
Check for the product code 18183390186 on the packaging. The product is a limited edition Key Lime Pie Ice Cream in a 473 ml pint size, labeled as gluten-free.
- Brand
Graeter's- Category
Food
What to do — step by step
Check Product Code
Look for the product code 18183390186 on the packaging to confirm if you have the recalled item.
Where it went and when
Where it was distributed
Distributed in 15 states.
FDA distribution: “Products were distributed in the following states: CA, FL, IL, IN, KY, MD, MI, NJ, NY, OH, PA, TX, UT, VA & WA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Florida, Illinois, Indiana, Kentucky, Maryland, Michigan, New Jersey, New York, Ohio, Pennsylvania, Texas, Utah, Virginia, Washington.
Recall timeline
FDA terminated this recall 7 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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-1837-2018 (August 7, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1837-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.