LaRosa's Creamy Garlic Dressing, 1.5oz plastic packet. Labeled in part, "INGREDIENTS: Soybean Oil, Water, Vinegar, Red Wine (preserved wi...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1383-2015.
The firm was notified by their customer that the ingredient statement on their packets of LaRosa Creamy Garlic Dressing and LaRosa Italian Dressing were switched. Therefore, rendering them to be misbranded due to undeclared Allergens of Milk, Egg and/or Sulfites.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1383-2015.
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 T. Marzetti Company 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-1383-2015.
T. Marzetti Company
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.
T. Marzetti Company Recall FAQ
T. Marzetti Company is the subject of a beverages safety report: LaRosa's Creamy Garlic Dressing, 1.5oz plastic packet. Labeled in part, "INGREDIENTS: Soybean Oil, Water, Vinegar, Red Wine (preserved wi.... The notice was published on February 12, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 732 units are potentially affected.