Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16-ounce glass jars, 6 jars per case. Shelf stable, refrige...
⚠ 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-0402-2023.
The firm has initiated a recall of Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi but containing vegetable minestrone, with an undeclared egg allergen.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0402-2023.
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 Sovos Brands Intermediate, Inc. 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-0402-2023.
SOVOS BRANDS INTERMEDIATE, INC.
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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.
Sovos Brands Intermediate, Inc. Recall FAQ
Sovos Brands Intermediate, Inc. is the subject of a meat & poultry safety report: Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16-ounce glass jars, 6 jars per case. Shelf stable, refrige.... The notice was published on January 27, 2023 by the U.S. Food and Drug Administration (FDA). Approximately 13,751 units are potentially affected.