RecallHawk
Class II Recall

simply to go Blueberry Yogurt Parfaits, 8.53oz, UPC 477088156552 and 477088150550; packaged in plastic cups

Sodexo Operations, LLC

Summary

The FDA issued a Class II for simply to go Blueberry Yogurt Parfaits, 8.53oz, UPC 477088156552 and 47708815055 by Sodexo Operations, LLC. Reason: Product contains undeclared soy lecithin and brown sugar syrup..

Details

Source

Food Recall

External ID

F-0972-2023

Action Date

2023-06-14

Status

Terminated

Category

food

Product Description

simply to go Blueberry Yogurt Parfaits, 8.53oz, UPC 477088156552 and 477088150550; packaged in plastic cups

Lot/Code Info: UPC: 477088156552 and 477088150550 Sell By Dates up to and including 05/08/2023

Quantity Affected: 23,059 plastic cups/units

Reason for Recall

Product contains undeclared soy lecithin and brown sugar syrup.

Distribution

MA, NH, RI

Type: Voluntary: Firm initiated

Recall Initiated: 2023-05-08

Company

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

Sodexo Operations, LLC 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 (Sodexo Operations, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Sodexo Operations, LLC have FDA actions?

Sodexo Operations, LLC 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-0972-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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