RecallHawk
Class II Recall

Dannon Plain Yogurt packaged in 32oz plastic carton with lid - 6 cartons per case

DANONE US LLC

Summary

The FDA issued a Class II for Dannon Plain Yogurt packaged in 32oz plastic carton with lid - 6 cartons per cas by DANONE US LLC. Reason: Potential contamination with sanitizer.

Details

Source

Food Recall

External ID

F-0871-2024

Action Date

2024-02-21

Status

Terminated

Category

food

Product Description

Dannon Plain Yogurt packaged in 32oz plastic carton with lid - 6 cartons per case

Lot/Code Info: Time Stamp - 13:40-13:55 Expiration 03/13/24

Quantity Affected: 15 cases (90 units)

Reason for Recall

Potential contamination with sanitizer

Distribution

Georgia

Type: Voluntary: Firm initiated

Recall Initiated: 2024-02-01

Company

DANONE US LLC

White Plains, NY

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

DANONE US LLC has 16 FDA actions in our database, including 16 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 (DANONE US LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does DANONE US LLC have FDA actions?

DANONE US LLC has 16 FDA actions in our database, including 16 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0871-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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