HEB Central Market Blueberry Buckwheat Gluten Free Waffle, 8.25oz, UPC 004122025365 Giant Eagle Blueberry Gluten Free Wa
Summary
The FDA issued a Class III for HEB Central Market Blueberry Buckwheat Gluten Free Waffle, 8.25oz, UPC 004122025 by Treehouse Foods. Reason: potentially contaminated with peanut.
Details
Source
Food Recall
External ID
F-0462-2024
Action Date
2023-11-29
Status
Terminated
Category
food
Product Description
HEB Central Market Blueberry Buckwheat Gluten Free Waffle, 8.25oz, UPC 004122025365 Giant Eagle Blueberry Gluten Free Waffle, 11.3oz, UPC 030034944940 Topco Full Circle Market Gluten Free Waffles - Blueberry, 11.3oz, UPC 036800486980
Lot/Code Info: Best By OCT 27 23, Batch 2C110272
Quantity Affected: 3966 cases (12 retail cartons per case)
Reason for Recall
potentially contaminated with peanut
Distribution
CA, IA, IL, OH, TX
Type: Voluntary: Firm initiated
Recall Initiated: 2023-10-18
Company
Oak Brook, IL
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Treehouse Foods has 69 FDA actions in our database, including 69 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (Treehouse Foods) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Treehouse Foods have FDA actions?
Treehouse Foods has 69 FDA actions in our database, including 69 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0462-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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