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