Lower riskFood recall · FDA · Published January 21, 2021
Door County Coffee & Tea Co. French Vanilla Cappuccino: Missing Allergen Info
Door County Coffee & Tea Co. recalls 10 single-serve French Vanilla Cappuccino cups due to missing allergen statements on retail boxes. Consumers should check lot codes and expiration dates.
“Door County Coffee & Tea Co. French Vanilla Cappuccino: Missing Allergen Info.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14899-door-county-coffee-tea-co-french-vanilla-cappuccino-missing-allergen. Based on FDA recall #F-0271-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0271-2021%22&limit=1).
The FDA announced on Jan. 21, 2021, that Door County Coffee & Tea Co., Inc. is recalling its French Vanilla Flavored Cappuccino because the retail box lacked an ingredient or allergen list. Owners should contact the company for a refund.
How to tell if you have it
Brand: Door County Coffee & Tea Co.
Product: French Vanilla Flavored Cappuccino, 10 Single Serve cups .51 oz (14g)/EA, Net Wt. 5.1 oz
Lot Code 1C092220-2, Expires 9/22/2022
Lot Code 1C120220-A, Expires 12/2/2022
Sold nationwide
The hazard
The retail box did not contain a list of ingredients or an allergen statement, according to the FDA.
Context
GovInfoNow's records show other recent recalls of similar products include Meijer Vanilla Bourbon Trail Mix Recalled for Undeclared Allergens (2026-04-21), Specialty Bakers Recalls Vanilla Dessert Shells Due to Undeclared Soy (2026-05-28), and Prime Food Lava Bun Green Tea Flavor Recall: Missing Milk Label (2025-11-16).
How to tell if you have this one
Check the retail box for the lot code and expiration date. The recalled cups have lot codes 1C092220-2 (expires 9/22/2022) or 1C120220-A (expires 12/2/2022).
Brand
Door County Coffee & Tea Co.
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Box for Allergen Info
Look for a list of ingredients or allergen statement on the retail box. If missing, the product is part of the recall.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0271-2021 (January 21, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0271-2021 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 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.