“Lidl Alpenfest Sachertote Recall: Undeclared Dairy and Wheat Ingredients.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/10684-lidl-alpenfest-sachertote-recall-undeclared-dairy-and-wheat-ingredients. Based on FDA recall #F-1448-2023 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1448-2023%22&limit=1).
The FDA announced on July 14, 2023, that Lidl US TRADING voluntarily recalled Alpenfest Style Sachertote due to undeclared egg, milk, and wheat allergens. Consumers should check their freezers for the product and contact the company for a refund.
How to tell if you have it
Brand: Lidl
Product: Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen Packaged in Cardboard Carton
UPC: 2010 0889
Expiration date: 15.03.2024
The hazard
The product contains undeclared egg, milk, and wheat, which can cause serious or unexpected allergic reactions in sensitive individuals. The recall is classified as Class II.
Context
GovInfoNow's records show Lidl US TRADING has 15 other recalls on record since September 13, 2018. Recent brand recalls include a March 12, 2026 recall of Favorina Chocolate Ladybugs Nougat due to unlabeled tree nuts and a July 22, 2026 recall of Greek Style Shortbread Cookies with undeclared allergens. Other recent recalls of similar products include Wawa Diet Iced Tea Lemon Pint Recall (April 2, 2026) and Loard's Lime Sherbert Recall (April 15, 2026).
How to tell if you have this one
Check for the UPC code 2010 0889 on the cardboard carton packaging. The product is a frozen Alpenfest Sachertote dessert with a net weight of 17.6 ounces (500g).
Brand
Lidl
Product
Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 Packaged in Cardboard Carton
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC code 2010 0889 on the cardboard carton packaging to identify affected items.
Where it went and when
Where it was distributed
Distributed in 9 states and D.C..
Listed by the agency
Not listed
FDA distribution: “Imported product directly shipped to a warehouse in Virginia and then distributed to 3 distribution centers in North Carolina, Virginia, and Maryland. From the distribution centers distributed to Lidl retail stores in Delaware, District of…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Delaware, District of Columbia, Georgia, Maryland, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, Virginia.
Recall timeline
FDA terminated this recall 46 days 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-1448-2023 (July 14, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1448-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.