RecallHawk
Class II Recall

Knorr Estrellitas con Tomate Tomato Based Star Pasta Soup Mix 3.5 oz UPC: 048001716193

Conopco DBA Unilever

Summary

The FDA issued a Class II for Knorr Estrellitas con Tomate Tomato Based Star Pasta Soup Mix 3.5 oz UPC: 048001 by Conopco DBA Unilever. Reason: Undeclared egg.

Details

Source

Food Recall

External ID

F-1514-2023

Action Date

2023-09-20

Status

Terminated

Category

food

Product Description

Knorr Estrellitas con Tomate Tomato Based Star Pasta Soup Mix 3.5 oz UPC: 048001716193

Lot/Code Info: Best buy dates prior to and including July 6, 2024

Quantity Affected: 215,000 cases

Reason for Recall

Undeclared egg

Distribution

Distributed nationwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-08-10

Company

Conopco DBA Unilever

Englewood Cliffs, NJ

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Conopco DBA Unilever has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Conopco DBA Unilever) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Conopco DBA Unilever have FDA actions?

Conopco DBA Unilever has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1514-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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