Rao's Made for Home Slow Simmered Soup recall
Recalled by Sovos Brands Intermediate, INC. · Louisville, CO, United States
Class I — High risk. Reasonable probability of serious harm or death.
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.
Undeclared allergen: Egg
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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.
Quantity: 13,751 cases
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
" Batch number: 046030Z009 " Lot number: 2320 " Packer or Manufacturer Number: MDV " Best By Date: Best By 11/15/2024
Where it was sold
Connecticut Florida Georgia Illinois Indiana Maryland Maine Michigan North Carolina Ohio Pennsylvania Texas
FDA's distribution note: The product was distributed to the following states: PA, MD, OH, MI, ME, CT TX, IN, IL,GA, NC and FL.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Sovos Brands Intermediate, INC.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 27, 2023
- In FDA report of
- Mar 1, 2023
- Terminated
- Jun 6, 2023
- FDA recall number
- F-0402-2023 · event 91626
- Official record
- FDA enforcement report search