Manischewitz Dark Chocolate Potato Chips Recall: Undeclared Peanuts, Tree Nuts, and Milk
Manischewitz recalls Dark Chocolate Potato Chips due to undeclared peanuts, tree nuts, and milk. Consumers should check for lot #1J026 and avoid if allergic.
Lower-risk recall
The R.A.B. Food Group LLC dba The Manischewitz Company, 80 Avenue K, Newark, NJ 07105 has initiated a recall of Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz. /12 per case. because of an undeclared allergen peanut, tree nut and milk.
Contact the company
What happened, in plain English
Manischewitz is recalling Dark Chocolate covered Potato Chips because they contain undeclared peanuts, tree nuts, and milk. This poses a risk for people with allergies to these ingredients. Read more at govinfonow.com/recall/19289-manischewitz-dark-chocolate-potato-chips-recall-undeclared-peanuts-tree-nuts.
Source Summary by GovInfoNow · govinfonow.com/recall/19289-manischewitz-dark-chocolate-potato-chips-recall-undeclared-peanuts-tree-nuts · Updated October 7, 2026 · FDA enforcement record: FDA #F-1542-2018
Cite this page
“Manischewitz Dark Chocolate Potato Chips Recall: Undeclared Peanuts, Tree Nuts, and Milk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19289-manischewitz-dark-chocolate-potato-chips-recall-undeclared-peanuts-tree-nuts. Based on FDA recall #F-1542-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1542-2018%22&limit=1).
Why it’s dangerous
The chips contain undeclared peanuts, tree nuts, and milk. This can cause allergic reactions in sensitive individuals, including potential anaphylaxis.
Who’s affected
People with peanut, tree nut, or milk allergies should avoid these chips. The recall affects consumers who purchased the specific lot number.
How to tell if you have this one
Check for the lot number 1J026 on the packaging. The product is sold in 4.25 oz bags, 12 per case, in mylar metalized bags inside gable boxes.
- Brand
Manischewitz- Category
Food
What to do — step by step
Check for Allergens
Look for the lot number 1J026 on the packaging to confirm if the product is recalled.
Where it went and when
Where it was distributed
Distributed in 11 states, and outside the U.S.
FDA distribution: “Distribution states MD, PA, WA, CT, NY, CO, CA, IL, NJ, FL, & MI, Ontatio Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Colorado, Connecticut, Florida, Illinois, Maryland, Michigan, New Jersey, New York, Pennsylvania, Washington.
Recall timeline
FDA terminated this recall 3.4 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- 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-1542-2018 (March 29, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1542-2018 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.