Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16-ounce glass jars, 6 jars per case. Shel
Summary
The FDA issued a Class I for Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16 by SOVOS BRANDS INTERMEDIATE, INC.. 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 u.
Details
Source
Food Recall
External ID
F-0402-2023
Action Date
2023-03-01
Status
Terminated
Category
food
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.
Lot/Code Info: " Batch number: 046030Z009 " Lot number: 2320 " Packer or Manufacturer Number: MDV " Best By Date: Best By 11/15/2024
Quantity Affected: 13,751 cases
Reason for Recall
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.
Distribution
The product was distributed to the following states: PA, MD, OH, MI, ME, CT TX, IN, IL,GA, NC and FL.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-01-27
Company
Louisville, CO
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 37 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (SOVOS BRANDS INTERMEDIATE, INC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SOVOS BRANDS INTERMEDIATE, INC. have FDA actions?
This is the only FDA action we have on record for SOVOS BRANDS INTERMEDIATE, INC. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0402-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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