Gourmet Old-Fashioned Caramel Holiday Popcorn, 18oz box, UPC 25606 00061
Summary
The FDA issued a Class II for Gourmet Old-Fashioned Caramel Holiday Popcorn, 18oz box, UPC 25606 00061 by Rieckhoff Family Businesses, Inc dba Cedar Creek Popcorn. Reason: Label contains "Gluten Free" claim but product contains wheat and barley which are declared on the label..
Details
Source
Food Recall
External ID
F-0142-2023
Action Date
2022-11-16
Status
Terminated
Category
food
Product Description
Gourmet Old-Fashioned Caramel Holiday Popcorn, 18oz box, UPC 25606 00061
Lot/Code Info: All lots and expiration dates
Quantity Affected: 20,870 boxes
Reason for Recall
Label contains "Gluten Free" claim but product contains wheat and barley which are declared on the label.
Distribution
Distribution Centers in AZ, GA, IN, KY, MD, NE, NY, and TX.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-10-27
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 66 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 (Rieckhoff Family Businesses, Inc dba Cedar Creek Popcorn) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Rieckhoff Family Businesses, Inc dba Cedar Creek Popcorn have FDA actions?
This is the only FDA action we have on record for Rieckhoff Family Businesses, Inc dba Cedar Creek Popcorn in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0142-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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