Stonewall Kitchen Cinnamon Sugar Doughnut Mix; Gluten Free; Home-Baked & Gluten Free; Net Wt. 18oz (510g); UPC: 11381313
Summary
The FDA issued a Class I for Stonewall Kitchen Cinnamon Sugar Doughnut Mix; Gluten Free; Home-Baked & Gluten by Stonewall Kitchen, LLC. Reason: Product contains undeclared wheat..
Details
Source
Food Recall
External ID
F-1082-2024
Action Date
2024-03-27
Status
Terminated
Category
food
Product Description
Stonewall Kitchen Cinnamon Sugar Doughnut Mix; Gluten Free; Home-Baked & Gluten Free; Net Wt. 18oz (510g); UPC: 1138131332
Lot/Code Info: Use By Dates: 3/9/25 and 3/10/25
Quantity Affected: 2405 units
Reason for Recall
Product contains undeclared wheat.
Distribution
MA, WY, MT, ND, IA, NC, NM, ME, NJ, VT, GA, MN, MI, MD, NV, DE, IN, UT, CA, TN, OH, PA, OR, WA, AZ, AR, SD, VA, FL, KY, NH, TX, IL, SC, MO. KS, NY, NE, WI, CO, ID, OK, CT, RI Ontario, Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2024-03-07
Company
York, ME
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 41 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Stonewall Kitchen, LLC has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Stonewall Kitchen, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Stonewall Kitchen, LLC have FDA actions?
Stonewall Kitchen, LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1082-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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