La Torre Marshmallow Chocolate Cookies Recall: Milk Not Listed on Label
La Torre Foods recalls marshmallow chocolate cookies due to milk not being listed on label despite calcium caseinate being declared. Consumers should check lot numbers for affected items.
Lower-risk recall
Calcium caseinate is declared on the label, but milk is not listed.
Contact the company
What happened, in plain English
La Torre Foods is recalling marshmallow chocolate cookies because milk isn't listed on the label even though calcium caseinate is declared. This could mean some people with milk allergies might be at risk of an allergic reaction. Read more at govinfonow.com/recall/23724-la-torre-marshmallow-chocolate-cookies-recall-milk-not-listed-on.
Source Summary by GovInfoNow · govinfonow.com/recall/23724-la-torre-marshmallow-chocolate-cookies-recall-milk-not-listed-on · Updated October 9, 2026 · FDA enforcement record: FDA #F-1973-2016
Cite this page
“La Torre Marshmallow Chocolate Cookies Recall: Milk Not Listed on Label.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23724-la-torre-marshmallow-chocolate-cookies-recall-milk-not-listed-on. Based on FDA recall #F-1973-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1973-2016%22&limit=1).
Why it’s dangerous
Calcium caseinate is a milk derivative used in the cookie. The label lists calcium caseinate but does not list milk, which could confuse consumers with milk allergies.
Who’s affected
People who have eaten or own the recalled cookies are at risk if they have milk allergies. Those with milk allergies should be cautious.
How to tell if you have this one
Check for cookies labeled 'La Torre Copito Marshmallow Chocolate Cookie' with net weight 4.94 oz in a cardboard box. Affected lots include 07 16, 09 16, 10 16, 12 16, 01 17, 03 17, 05 17.
- Brand
La Torre- Category
Food
What to do — step by step
Check Label for Milk
Look for the label that lists calcium caseinate but not milk on the cookie packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide throughout the US.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 9 months 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-1973-2016 (July 26, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1973-2016 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.