May Flower 3+2 Soda Crackers Cream Flavour Recall: Undeclared Milk
May Flower International recalls 3+2 Soda Crackers (Cream Flavour) due to undeclared milk content. Consumers should check for yellow 4.4oz packages with UPC 6919892633101.
Lower-risk recall
Product contains undeclared milk.
Contact the company
What happened, in plain English
May Flower is recalling 3+2 Soda Crackers in Cream Flavour because they contain undeclared milk. This affects people with milk allergies who might react to the milk in the crackers. Read more at govinfonow.com/recall/19016-may-flower-3-2-soda-crackers-cream-flavour-recall-undeclared.
Source Summary by GovInfoNow · govinfonow.com/recall/19016-may-flower-3-2-soda-crackers-cream-flavour-recall-undeclared · Updated October 6, 2026 · FDA enforcement record: FDA #F-1676-2018
Cite this page
“May Flower 3+2 Soda Crackers Cream Flavour Recall: Undeclared Milk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/19016-may-flower-3-2-soda-crackers-cream-flavour-recall-undeclared. Based on FDA recall #F-1676-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1676-2018%22&limit=1).
Why it’s dangerous
The crackers contain undeclared milk, meaning they might cause allergic reactions in people who are sensitive to milk. This is a food safety issue for those with milk allergies.
Who’s affected
People with milk allergies are most at risk from this recall. The product is sold in yellow 4.4-ounce packages with a specific UPC code.
How to tell if you have this one
Check for yellow 4.4 oz packages labeled '3+2 Soda Crackers (Cream Flavour)' with UPC 6919892633101. The product has no other codes or identifiers.
- Brand
May Flower- Product
May Flower International Inc. recalls 3+2 Soda Crackers (CREAM FLAVOUR)(S) packaged in a 4.4 oz, yellow package, UPC: 6 919892 633101- Category
Food
What to do — step by step
Check Product Details
Look for the yellow 4.4 oz package with UPC 6919892633101 to confirm if you have the recalled item.
Where it went and when
Where it was distributed
Distributed in New York.
FDA distribution: “New York” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New York.
Recall timeline
FDA terminated this recall 34 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-1676-2018 (June 29, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1676-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.