GOODMAN GLUTEN FREE; Vegan Apple Pie, Fully Baked 16.4 oz, paperboard box; INGREDIENTS: Apples, Potato Starch, Palm Oil,
Summary
The FDA issued a Class III for GOODMAN GLUTEN FREE; Vegan Apple Pie, Fully Baked 16.4 oz, paperboard box; INGRE by Goodman Food Products LLC. Reason: Product contains undeclared cinnamon..
Details
Source
Food Recall
External ID
F-1416-2022
Action Date
2022-07-20
Status
Terminated
Category
food
Product Description
GOODMAN GLUTEN FREE; Vegan Apple Pie, Fully Baked 16.4 oz, paperboard box; INGREDIENTS: Apples, Potato Starch, Palm Oil, Sugar, Brown Rice Flour, White Rice Flour, Dextrose, Xanthan Gum, Salt. Processed in a facility that also processes: Egg, Tree Nuts; Manufactured for GOODMAN FOOD PRODUCTS, LLC MADISON, CT 06443
Lot/Code Info: UPC Code 8-57176-00828-2 Lot Numbers: 22088,22089,22118
Quantity Affected: 820 cases
Reason for Recall
Product contains undeclared cinnamon.
Distribution
NC, SC, NJ
Type: Voluntary: Firm initiated
Recall Initiated: 2022-06-19
Company
Madison, CT
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 41 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Goodman Food Products LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Goodman Food Products LLC have FDA actions?
This is the only FDA action we have on record for Goodman Food Products LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1416-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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