Request Foods GFS Cheese Manicotti in Tomato Sauce Recall: Undeclared Eggs
Request Foods recalls GFS Cheese Manicotti in tomato sauce due to undeclared eggs. This product may contain eggs not listed on the label, posing a risk for those with egg allergies.
Lower-risk recall
Undeclared Eggs
Contact the company
What happened, in plain English
Request Foods is recalling GFS Cheese Manicotti in tomato sauce because it contains undeclared eggs. This poses a risk for people with egg allergies who might consume the product without knowing. Read more at govinfonow.com/recall/22874-request-foods-gfs-cheese-manicotti-in-tomato-sauce-recall-undeclared.
Source Summary by GovInfoNow · govinfonow.com/recall/22874-request-foods-gfs-cheese-manicotti-in-tomato-sauce-recall-undeclared · Updated October 8, 2026 · FDA enforcement record: FDA #F-0723-2017
Cite this page
“Request Foods GFS Cheese Manicotti in Tomato Sauce Recall: Undeclared Eggs.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22874-request-foods-gfs-cheese-manicotti-in-tomato-sauce-recall-undeclared. Based on FDA recall #F-0723-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0723-2017%22&limit=1).
Why it’s dangerous
The product contains eggs that are not listed on the label. This can cause allergic reactions in individuals who are sensitive or allergic to eggs. The risk is specific to those with egg allergies.
Who’s affected
People who have purchased this cheese product are likely affected. Those with egg allergies are at the highest risk due to potential exposure to undeclared eggs.
How to tell if you have this one
Check for the product name 'GFS Cheese Manicotti in tomato sauce' with a 68 oz. pan. The lot code is 15268 and UPC is 9390121983.
- Brand
Request Foods- Product
GFS Cheese Manicotti in tomato sauce. retail 68 oz. pan. 4 retail units per case- Category
Food
What to do — step by step
Check Product Label
Look for the lot code 15268 and UPC 9390121983 on the product label.
Where it went and when
Where it was distributed
Distributed in 4 states.
FDA distribution: “MI, OH, FL, KY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Kentucky, Michigan, Ohio.
Recall timeline
FDA terminated this recall 8 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- 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-0723-2017 (November 15, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0723-2017 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.