Meijer No Salt Potato Chips Recall: Undeclared Milk and Soy Allergens
Shearers Foods recalls Meijer brand No Salt Added Original Kettle Cooked Potato Chips due to undeclared milk and soy allergens. Consumers should check lot numbers and contact Meijer for details.
Lower-risk recall
Undeclared allergens: milk (whey) and soy.
Contact the company
What happened, in plain English
Shearers Foods is recalling Meijer brand No Salt Added Original Kettle Cooked Potato Chips because they contain undeclared milk (whey) and soy allergens. This poses a risk for people with allergies to these ingredients. Read more at govinfonow.com/recall/23226-meijer-no-salt-potato-chips-recall-undeclared-milk-and-soy.
Source Summary by GovInfoNow · govinfonow.com/recall/23226-meijer-no-salt-potato-chips-recall-undeclared-milk-and-soy · Updated October 9, 2026 · FDA enforcement record: FDA #F-0617-2017
Cite this page
“Meijer No Salt Potato Chips Recall: Undeclared Milk and Soy Allergens.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23226-meijer-no-salt-potato-chips-recall-undeclared-milk-and-soy. Based on FDA recall #F-0617-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0617-2017%22&limit=1).
Why it’s dangerous
The chips contain undeclared milk (whey) and soy allergens. For individuals with allergies to these ingredients, consuming the product could cause an allergic reaction.
Who’s affected
People with milk or soy allergies are at risk from these potato chips. The recall affects consumers who purchased the Meijer brand product from stores like Meijer.
How to tell if you have this one
Check for the Meijer brand No Salt Added Original Kettle Cooked Potato Chips in 8.5oz bags. The lot number is OCT 31 2016 with an expiration date of 10/31/2016.
- Brand
Shearers Foods- Category
Food
What to do — step by step
Check Product Details
Look for the Meijer brand No Salt Added Original Kettle Cooked Potato Chips in 8.5oz bags with lot number OCT 31 2016.
Where it went and when
Where it was distributed
Distributed in Michigan.
FDA distribution: “The product was distributed to the following states: MI.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Michigan.
Recall timeline
FDA terminated this recall 11 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-0617-2017 (September 8, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0617-2017 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.