Class ITerminated in FDA datasetRecall initiated Jan 27, 2023

Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16-ounce glass…

Recalling firm: SOVOS BRANDS INTERMEDIATE, INC.

Why it was recalled

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.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jun 6, 2023.

Check your package

Compare the exact product and package details with the label you have.

ProductRao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16-ounce glass jars, 6 jars per case. Shelf stable, refrigerate after opening.

FDA code information

" Batch number: 046030Z009 " Lot number: 2320 " Packer or Manufacturer Number: MDV " Best By Date: Best By 11/15/2024

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16-ounce glass jars, 6 jars per case. Shelf stable, refrigerate after opening.

Extracted codes and context

TypeCode / valueContext
batch046030Z009" Batch number: 046030Z009 " Lot number: 2320 " Packer or Manufacturer Number: MDV " Best By Date: Best By 11/15/2024
best by11/15/2024" Lot number: 2320 " Packer or Manufacturer Number: MDV " Best By Date: Best By 11/15/2024
lot2320" Batch number: 046030Z009 " Lot number: 2320 " Packer or Manufacturer Number: MDV " Best By Date: Best By 11/15/2024

Original FDA recall reason

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.

Recall details

Recall number
F-0402-2023
Event ID
91626
FDA status
Terminated
Initiated
Jan 27, 2023
Reported
Mar 1, 2023
Classified
Mar 3, 2023
Terminated
Jun 6, 2023
Quantity
13,751 cases
Location
Louisville, CO, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

The product was distributed to the following states: PA, MD, OH, MI, ME, CT TX, IN, IL,GA, NC and FL.

FDA source record · F-0402-2023

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.