Class II Recall

SoDelicious DairyFree Wondermilk Dairy Free Frozen Dessert Salted Caramel Sundae, 3 - 4 fl oz (12 fl oz) cones per carto

Summary

The FDA issued a Class II for SoDelicious DairyFree Wondermilk Dairy Free Frozen Dessert Salted Caramel Sundae by DANONE US LLC. Reason: A small number of individual cones with peanut pieces were mistakenly packed into a few cartons of Salted Caramel Sundae which does not have peanuts..

Details

Source

Food Recall

External ID

F-1400-2022

Action Date

2022-07-13

Status

Terminated

Product Description

SoDelicious DairyFree Wondermilk Dairy Free Frozen Dessert Salted Caramel Sundae, 3 - 4 fl oz (12 fl oz) cones per carton. UPC 0 36632 07821 6 Manufactured by/for: So Delicious Dairy Free, Eugene, OR 97402. Keep frozen.

Lot/Code Info: Best if Used by: 15 June 2023

Quantity Affected: 5,471 cases (6 cartons per case)

Reason for Recall

A small number of individual cones with peanut pieces were mistakenly packed into a few cartons of Salted Caramel Sundae which does not have peanuts.

Distribution

AZ; CA; CO; FL; IA; KY; MA; MD; NH; NY; PA; TX; UT; WI

Type: Voluntary: Firm initiated

Recall Initiated: 2022-06-21

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 53 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-1400-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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