Dakota Honey Company Spreadable Spun Honey
Recalled by Dakota Honey Company
Food recall
Dakota Honey Company
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Dakota Honey Company has recalled Dakota Honey Company Spreadable Spun Honey, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on May 20, 2026 and was initiated on April 4, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Dakota Honey Company Spreadable Spun Honey, with approximately 1897 - 4 oz containers, and 286 - 12 oz containers Total. affected. The company behind the recall is Dakota Honey Company, based in Winner, SD. The FDA describes the product as: “Dakota Honey Company Spreadable Spun Honey, Salted Caramel. Stir before use. Produced in Winner, SD. Packaged in the following sized plastic jars: 1. Net Wt 4 oz (113g) UPC 8 60012-41981 4. 2. Net Wt 12 oz (340g) UPC 8 60010-57964 0.”
Why was Dakota Honey Company Spreadable Spun Honey recalled?
According to the FDA, the stated reason for the recall is: “Foreign object (stainless steel dust/flakes or shreds of plastic).” In plain terms, this recall relates to foreign material.
A foreign material recall means that pieces of something which should not be in food — such as metal, plastic, or glass — may be present. These can pose a choking hazard or cause injury. Recalls like these are issued to remove the affected product before anyone is hurt.
What should you do?
If you think you may have bought Dakota Honey Company Spreadable Spun Honey, compare it against the product description and identifying codes (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,…) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Dakota Honey Company or your local health authority.
About this recall
This recall was distributed in SD. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Ongoing
- Date reported
- May 20, 2026
- Recall started
- April 4, 2026
- Distributed in
- SD
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Dakota Honey Company Spreadable Spun Honey recalled?+
According to the FDA: Foreign object (stainless steel dust/flakes or shreds of plastic)
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Dakota Honey Company Spreadable Spun Honey?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0770-2026. Information last synced from the FDA on July 6, 2026.