BON APPETITO Walnut Ladies Finger Recall: Undeclared Eggs and Soy Oil
BON APPETITO recalls 10oz walnut fingers due to undeclared eggs and soy lecithin. Consumers should check UPC 644744698767 for affected products.
Lower-risk recall
Undeclared Eggs and Soy Oil/Lecithin
Contact the company
What happened, in plain English
BON APPETITO is recalling 10oz walnut fingers because they contain undeclared eggs and soy lecithin. This could cause allergic reactions in people with egg or soy allergies. The recall affects products with UPC 644744698767 sold before November 14, 2016. Read more at govinfonow.com/recall/22958-bon-appetito-walnut-ladies-finger-recall-undeclared-eggs-and-soy.
Source Summary by GovInfoNow · govinfonow.com/recall/22958-bon-appetito-walnut-ladies-finger-recall-undeclared-eggs-and-soy · Updated October 9, 2026 · FDA enforcement record: FDA #F-0610-2017
Cite this page
“BON APPETITO Walnut Ladies Finger Recall: Undeclared Eggs and Soy Oil.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/22958-bon-appetito-walnut-ladies-finger-recall-undeclared-eggs-and-soy. Based on FDA recall #F-0610-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0610-2017%22&limit=1).
Why it’s dangerous
These products contain eggs and soy lecithin without being listed on the label. This can cause allergic reactions in people who are sensitive to eggs or soy. The recall is for products sold before November 14, 2016.
Who’s affected
People with egg or soy allergies may react to these products. The recall affects BON APPETITO walnut fingers sold in the U.S. with UPC 644744698767 before November 14, 2016.
How to tell if you have this one
Check for the UPC 644744698767 on the product label. The product is a 10oz walnut finger with an expiration date of November 14, 2016.
- Brand
BON APPETITO- Product
BON APPETITO WALNUT LADIES FINGER, Net Wt.: 10oz. (340g), UPC 6 44744 69876 7- Category
Food
What to do — step by step
Check Product Label
Look for the UPC 644744698767 on the label to identify affected products.
Where it went and when
Where it was distributed
Distributed in New Jersey and New York.
FDA distribution: “NY & NJ” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New Jersey, New York.
Recall timeline
FDA terminated this recall 20 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-0610-2017 (November 1, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0610-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.