Fairway Candy Corn Recall: Undeclared Egg Risk
Fairway Bakery recalls Candy Corn products due to potential undeclared egg content. Consumers should check packaging for item code 228402 and return items if purchased.
Lower-risk recall
The product may contain undeclared egg.
Contact the company
What happened, in plain English
Fairway Bakery is recalling Candy Corn products that may contain undeclared egg. This poses a risk for people with egg allergies who could experience an allergic reaction. Read more at govinfonow.com/recall/22766-fairway-candy-corn-recall-undeclared-egg-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/22766-fairway-candy-corn-recall-undeclared-egg-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-0818-2017
Cite this page
“Fairway Candy Corn Recall: Undeclared Egg Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22766-fairway-candy-corn-recall-undeclared-egg-risk. Based on FDA recall #F-0818-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0818-2017%22&limit=1).
Why it’s dangerous
The product may contain undeclared egg, which can cause allergic reactions in sensitive individuals. This is a food safety issue for those with egg allergies.
Who’s affected
People with egg allergies are at risk of an allergic reaction from this product. Consumers who purchased Candy Corn with item code 228402 should check their packaging.
How to tell if you have this one
Check for the item code 228402 on the packaging. The product is sold in clear plastic cello bags weighing less than one pound.
- Brand
Fairway Bakery- Category
Food
What to do — step by step
Check Packaging
Look for item code 228402 on the packaging to identify recalled Candy Corn products.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “New York, New Jersey and Connecticut and via the internet” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Connecticut, New Jersey, New York.
Recall timeline
FDA terminated this recall 18 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-0818-2017 (December 6, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0818-2017 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.