Heinen's Potato Gnocchi Recall: Undeclared Milk Allergen Risk
Heinen's Potato Gnocchi (9 oz. preservative-free) recalled due to undeclared milk allergen. Consumers should check lot numbers on clear plastic trays.
Use caution until it’s fixed
LA PASTA, INC has initiated a recall of Heinen's Potato Gnocchi 9 oz. , because of a undeclared milk allergen .
Contact the company
What happened, in plain English
Heinen's Potato Gnocchi in clear plastic trays is recalled because it contains an undeclared milk allergen. This poses a risk for people with milk allergies. Read more at govinfonow.com/recall/19639-heinen-s-potato-gnocchi-recall-undeclared-milk-allergen-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/19639-heinen-s-potato-gnocchi-recall-undeclared-milk-allergen-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0909-2018
Cite this page
“Heinen's Potato Gnocchi Recall: Undeclared Milk Allergen Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19639-heinen-s-potato-gnocchi-recall-undeclared-milk-allergen-risk. Based on FDA recall #F-0909-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0909-2018%22&limit=1).
Why it’s dangerous
The product contains milk as an allergen that was not listed on the label. This can cause allergic reactions in people sensitive to milk, including potentially serious reactions.
Who’s affected
People with milk allergies are at risk from this product. Anyone who purchased the recalled Heinen's Potato Gnocchi in clear plastic trays should check if they have the affected lot numbers.
How to tell if you have this one
Check the clear plastic trays for lot numbers: 1119-1120, 1121-1122, 1132-1133, 2016-2017, 2027-2028, 2034-2035, 2038-2039, 2130-2131, 2139-2140, 2221-2222, or 2231-2232.
- Brand
Heinen's- Category
Food
What to do — step by step
Check Product Lot Number
Look for lot numbers on the clear plastic tray: 1119-1120, 1121-1122, 1132-1133, 2016-2017, 2027-2028, 2034-2035, 2038-2039, 2130-2131, 2139-2140, 2221-2222, or 2231-2232.
Where it went and when
Where it was distributed
Distributed in Illinois and Ohio.
FDA distribution: “The product was distributed to the following states IL and OH” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois, Ohio.
Recall timeline
FDA terminated this recall 3 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-0909-2018 (February 21, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0909-2018 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.