Stewart's Shops Cranberry Apple Refresher 16oz Recall: Undeclared Milk
Stewart's Shops recalls Cranberry Apple Refresher 16oz (UPC 082086310143) due to undeclared milk. Consumers should check if they have this product and contact the company for details.
Lower-risk recall
Product contains undeclared milk.
Contact the company
What happened, in plain English
Stewart's Shops is recalling their Cranberry Apple Refresher 16oz drink because it contains undeclared milk. This could cause allergic reactions for people who are lactose intolerant or allergic to milk. Read more at govinfonow.com/recall/18272-stewart-s-shops-cranberry-apple-refresher-16oz-recall-undeclared-milk.
Source Summary by GovInfoNow · govinfonow.com/recall/18272-stewart-s-shops-cranberry-apple-refresher-16oz-recall-undeclared-milk · Updated October 5, 2026 · FDA enforcement record: FDA #F-0416-2019
Cite this page
“Stewart's Shops Cranberry Apple Refresher 16oz Recall: Undeclared Milk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/18272-stewart-s-shops-cranberry-apple-refresher-16oz-recall-undeclared-milk. Based on FDA recall #F-0416-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0416-2019%22&limit=1).
Why it’s dangerous
The product contains milk without being declared on the label. This can cause allergic reactions in people who are sensitive to milk, including those with lactose intolerance or milk allergies.
Who’s affected
People who have consumed or own this product may be at risk of allergic reactions if they are lactose intolerant or allergic to milk. Those with milk allergies are most at risk.
How to tell if you have this one
Check for the product name 'Cranberry Apple Refresher', 16oz size, and UPC 082086310143. The product was sold starting November 19.
- Brand
Stewart's Shops- Product
Stewart's Shops, CRANBERRY APPLE REFRESHER, 16 oz., UPC: UPC 0 82086 31014 3- Category
Food
What to do — step by step
Check Product Details
Look for the product name 'Cranberry Apple Refresher', 16oz size, and UPC 082086310143.
Where it went and when
Where it was distributed
Distributed in New York and Vermont.
FDA distribution: “NY and VT” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New York, Vermont.
Recall timeline
FDA terminated this recall 27 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- FDA terminated the recall
- Published in FDA’s Enforcement Report
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-0416-2019 (October 17, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0416-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.