Good Eggs SF Bay Panang Curry Dinner: Peanuts Missing from Allergen List
Good Eggs SF Bay recalls Panang Curry dinner due to peanuts not listed as an allergen despite being an ingredient. This poses a risk for those with peanut allergies.
Lower-risk recall
Panang Curry included in the Beef Panang Curry Dinner does not list peanuts as an allergen, although peanuts are listed as an ingredient.
Contact the company
What happened, in plain English
Good Eggs SF Bay is recalling their Panang Curry dinner because peanuts are an ingredient but not listed as an allergen. This could cause allergic reactions in people sensitive to peanuts. Read more at govinfonow.com/recall/20439-good-eggs-sf-bay-panang-curry-dinner-peanuts-missing-from.
Source Summary by GovInfoNow · govinfonow.com/recall/20439-good-eggs-sf-bay-panang-curry-dinner-peanuts-missing-from · Updated October 7, 2026 · FDA enforcement record: FDA #F-0010-2018
Cite this page
“Good Eggs SF Bay Panang Curry Dinner: Peanuts Missing from Allergen List.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20439-good-eggs-sf-bay-panang-curry-dinner-peanuts-missing-from. Based on FDA recall #F-0010-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0010-2018%22&limit=1).
Why it’s dangerous
The product contains peanuts but fails to list them as an allergen. This means individuals with peanut allergies might consume the product without knowing, leading to potential allergic reactions.
Who’s affected
People who have purchased the Panang Curry dinner with peanuts as an ingredient but the allergen list does not include peanuts. Those with peanut allergies are at higher risk.
How to tell if you have this one
Check for the 3.5 oz. 8oz plastic deli container labeled 'Curry Paste' in the Beef Panang Curry Dinner. The product was sold with a use-by date of September 8, 2017.
- Brand
Good Eggs SF - Bay- Category
Food
What to do — step by step
Check Allergen List
Review the product's allergen list to confirm peanuts are included.
Where it went and when
Where it was distributed
Distributed in California.
FDA distribution: “Direct customers in Bay Area of CA only.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California.
Recall timeline
FDA terminated this recall 56 days 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-0010-2018 (September 7, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0010-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.