RecallHawk
Class II Recall

Creekside Mallow Chocolate Chip Mint Marshmallows, packed in a Stand Up Flexible Pouch (Bag), Net wt. 3.9oz. UPC 7 09951

CREEKSIDE MALLOW LLC

Summary

The FDA issued a Class II for Creekside Mallow Chocolate Chip Mint Marshmallows, packed in a Stand Up Flexible by CREEKSIDE MALLOW LLC. Reason: Butterfat is declared in the Ingredients Statement, but MILK is not declared in the Contains statement..

Details

Source

Food Recall

External ID

F-0751-2023

Action Date

2023-05-03

Status

Terminated

Category

food

Product Description

Creekside Mallow Chocolate Chip Mint Marshmallows, packed in a Stand Up Flexible Pouch (Bag), Net wt. 3.9oz. UPC 7 09951 63271 0. Manufactured by Creekside Mallow LLC Caldwell, ID. www.creeksidemallow.com. The label declares: INGREDIENTS: CORN SYRUP ***SUGAR, WATER, CHOCOLATE CHIPS (SUGAR, CHOCOLATE LIQUOR, COCOA BUTTER, BUTTERFAT, SOY LECITHIN, NATURAL FLAVOR)***CONTAINS: SOY.

Lot/Code Info: All codes and dates (DDMMYY). New product NOT subject to recall will have the statement "Contains: MILK, SOY".

Quantity Affected: 2800 packages

Reason for Recall

Butterfat is declared in the Ingredients Statement, but MILK is not declared in the Contains statement.

Distribution

Distributed in Washington.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-04-13

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

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

How often does CREEKSIDE MALLOW LLC have FDA actions?

This is the only FDA action we have on record for CREEKSIDE MALLOW LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0751-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions