Sid Wainer & Son Dried Chili Peppers Recall: Undeclared Peanuts Hazard
Sid Wainer & Son recalls 1-oz dried chili peppers with undeclared peanuts. Consumers should avoid these products to prevent allergic reactions.
Lower-risk recall
Product contains undeclared peanuts
Contact the company
What happened, in plain English
Sid Wainer & Son is recalling 1-ounce dried chili peppers from the Jansal Valley brand due to undeclared peanuts. This poses a risk for people with peanut allergies who might accidentally consume the product. Read more at govinfonow.com/recall/20393-sid-wainer-son-dried-chili-peppers-recall-undeclared-peanuts-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/20393-sid-wainer-son-dried-chili-peppers-recall-undeclared-peanuts-hazard · Updated October 7, 2026 · FDA enforcement record: FDA #F-0086-2018
Cite this page
“Sid Wainer & Son Dried Chili Peppers Recall: Undeclared Peanuts Hazard.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20393-sid-wainer-son-dried-chili-peppers-recall-undeclared-peanuts-hazard. Based on FDA recall #F-0086-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0086-2018%22&limit=1).
Why it’s dangerous
The dried chili peppers contain undeclared peanuts, meaning they are not labeled as peanut-free. This can cause allergic reactions in individuals with peanut allergies who might unknowingly eat the product.
Who’s affected
People with peanut allergies are at risk of allergic reactions if they accidentally consume these peppers. The product is sold in plastic clamshell containers.
How to tell if you have this one
Check for Sid Wainer & Son Jansal Valley brand dried chili peppers in 1-ounce plastic clamshell containers. Lot numbers 6863 with best by dates 9/11/2018, 9/22/2018, or 9/26/2018.
- Brand
Sid Wainer & Son- Category
Food
What to do — step by step
Check Product Label
Look for the lot number 6863 and best by dates 9/11/2018, 9/22/2018, or 9/26/2018 on the plastic clamshell container.
Where it went and when
Where it was distributed
Distributed in 4 states.
FDA distribution: “MA, NJ, RI, GA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Georgia, Massachusetts, New Jersey, Rhode Island.
Recall timeline
FDA terminated this recall 35 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- FDA terminated the recall
- Published in FDA’s Enforcement Report
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-0086-2018 (October 2, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0086-2018 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.