Hors D'Oeuvre, Holiday Foods¿ Breaded Macaroni and Cheese Bites with Quattro Formaggi Cheese, Lobster & Truffle Oil (item number 4802732)...
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0790-2015.
Schwan's Global Supply Chain, Inc. is recalling three Holiday Foods¿ products. This recall has been initiated because the products contain undeclared anchovy, an element of the Worcestershire sauce used in the finished product. People who have an allergy or severe sensitivity to fish run the risk of serious or life-threatening allergic reaction if they consume these products. There have been no re
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0790-2015.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Schwan Food Company Dba Holiday Foods or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0790-2015.
Schwan Food Company dba Holiday Foods
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Schwan Food Company Dba Holiday Foods Recall FAQ
Schwan Food Company Dba Holiday Foods is the subject of a dairy safety report: Hors D'Oeuvre, Holiday Foods¿ Breaded Macaroni and Cheese Bites with Quattro Formaggi Cheese, Lobster & Truffle Oil (item number 4802732).... The notice was published on December 15, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 27 units are potentially affected.