Ronzoni Thin Spaghetti Recall: Undeclared Egg in Some Products
Riviana International recalls Ronzoni Thin Spaghetti (UPC 71300 00009) due to undeclared egg content. Consumers should check product codes and contact the company for details.
Lower-risk recall
Undeclared egg. One lot Ronzoni Thin Spaghetti contained Ronzoni Egg Fettuccine.
Contact the company
What happened, in plain English
Riviana International is recalling some Ronzoni Thin Spaghetti products because they contain undeclared egg. This could affect people with egg allergies who might experience a reaction. The recall is for specific products with a unique UPC code. Read more at govinfonow.com/recall/21992-ronzoni-thin-spaghetti-recall-undeclared-egg-in-some-products.
Source Summary by GovInfoNow · govinfonow.com/recall/21992-ronzoni-thin-spaghetti-recall-undeclared-egg-in-some-products · Updated October 8, 2026 · FDA enforcement record: FDA #F-1965-2017
Cite this page
“Ronzoni Thin Spaghetti Recall: Undeclared Egg in Some Products.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21992-ronzoni-thin-spaghetti-recall-undeclared-egg-in-some-products. Based on FDA recall #F-1965-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1965-2017%22&limit=1).
Why it’s dangerous
The recalled products contain egg that was not listed on the label. This can cause allergic reactions in people who are sensitive or allergic to eggs. The risk is limited to those with egg allergies.
Who’s affected
People with egg allergies may react to the undeclared egg in these products. Most consumers are not at risk unless they have a known egg allergy.
How to tell if you have this one
Check for the UPC code 71300 00009 on the product label. Products were sold with the code JAN 20 19 K.
- Brand
Ronzoni- Product
Ronzoni(R) Thin Spaghetti, NO. 9, ENRICHED MACARONI PRODUCT, NET WT 16 OA (454g)., UPC 71300 00009- Category
Food
What to do — step by step
Check Product Label
Look for the UPC code 71300 00009 on the packaging.
Where it went and when
Where it was distributed
Distributed in Florida and Pennsylvania.
FDA distribution: “PA and FL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Pennsylvania.
Recall timeline
FDA terminated this recall 5 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-1965-2017 (March 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1965-2017 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.