Recall record at a glance
| Official record | F-1242-2023 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Dakota Style, Inc. |
| Report date | Jul 19, 2023 |
| Recall initiation date | Apr 13, 2023 |
| Quantity | 334,357 total bags |
| Location | Clark, SD, United States |
Official product description
1. Hy-Vee Honey Mustard Braided Pretzels, 10oz poly bags, UPC: 75450-24309, 12 pack; 2. Dakota Style Honey Mustard Pretzel Kravings, 10oz poly bags, UPC 84872-60031, 12 pack and 6 pack; 3. Four Brothers Honey Mustard Pretzels, 10oz poly bags, UPC: 33147-89145, 12 pack; 4. Schnucks Honey Mustard Pretzels Schticks, 10oz poly bag, UPC: 41318-25266, 12 pack; 5. Best Choice Honey Mustard Pretzel Twists, 10oz poly bags, UPC: 70038-66479, 12 pack; 6. Gelson's Honey Mustard Pretzels, 4.5oz poly bags, UPC: 23621-11186, 12 pack; 7. PICS / Price Chopper Honey Mustard Pretzel Twists, 10oz poly bag, UPC: 41735-05739, 12 pack; 8. Stadium Honey Mustard Pretzels, 2oz. poly bags, UPC: 60003-51999, 80 pack
Why the product was recalled
May contain undeclared milk
Distribution information
Nationwide
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Telephone.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.