Dakota Honey Company Spreadable Spun Honey, Cinnamon-Infused. Stir before use. Produced in Winner, SD. Packaged in t
Summary
The FDA issued a Class II for Dakota Honey Company Spreadable Spun Honey, Cinnamon-Infused. Stir before use. by Dakota Honey Company. Reason: Foreign object (stainless steel dust/flakes or shreds of plastic).
Details
Source
Food Recall
External ID
H-0769-2026
Action Date
2026-05-20
Status
Ongoing
Category
food
Product Description
Dakota Honey Company Spreadable Spun Honey, Cinnamon-Infused. Stir before use. Produced in Winner, SD. Packaged in the following sized plastic jars: 1. Net Wt 4 oz (113g) UPC 8 60012-41980 7. 2. Net Wt 12 oz (340g) UPC 8 60010-57963 3.
Lot/Code Info: Honey does not have any code on container. 1. 4 oz spun honey purchased from December 19, 2025 to April 3, 2026 2. 12 oz spun honey purchased from February 25, 2026 to April 3, 2026
Quantity Affected: 1897 - 4 oz containers and 286 - 12 oz containers Total.
Reason for Recall
Foreign object (stainless steel dust/flakes or shreds of plastic)
Distribution
Retail locations in FL, GA, and SD Internet sales Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-04
Company
Winner, SD
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 97 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Dakota Honey Company has 5 FDA actions in our database, including 5 recalls.
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 (Dakota Honey Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Dakota Honey Company have FDA actions?
Dakota Honey Company has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0769-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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