RecallHawk
Class II Recall

Curry Vinaigrette; Made with Yellow Onion Item number 7020 Refrigerated

Mosaic Food Company

Summary

The FDA issued a Class II for Curry Vinaigrette; Made with Yellow Onion Item number 7020 Refrigerated by Mosaic Food Company. Reason: Product was manufactured with onions recalled for Salmonella contamination..

Details

Source

Food Recall

External ID

F-1048-2022

Action Date

2022-05-18

Status

Terminated

Category

food

Product Description

Curry Vinaigrette; Made with Yellow Onion Item number 7020 Refrigerated

Lot/Code Info: lot 24421

Quantity Affected: 54 cases

Reason for Recall

Product was manufactured with onions recalled for Salmonella contamination.

Distribution

CA

Type: Voluntary: Firm initiated

Recall Initiated: 2021-11-10

Company

Mosaic Food Company

El Segundo, CA

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 29 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Mosaic Food Company has 2 FDA actions in our database, including 2 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 (Mosaic Food Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Mosaic Food Company have FDA actions?

Mosaic Food Company has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1048-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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