📍Recalling firmLyons Magnus, Inc3158 E Hamilton Ave · Fresno, CA 93702-4163
✎ GovInfoNow plain-language explainer
Lyons Magnus, Inc. is recalling Dunkin Caramel Swirl syrup because the individual containers inside the case are incorrectly labeled as Dunkin Mocha Swirl. This mislabeling fails to declare milk as an allergen, posing a risk to consumers with milk allergies. The affected product was distributed initially to Arizona. Read more at govinfonow.com/recall/13369-recall-dunkin-caramel-swirl-syrup-undeclared-milk-allergen.
“Recall: Dunkin Caramel Swirl Syrup Undeclared Milk Allergen.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/13369-recall-dunkin-caramel-swirl-syrup-undeclared-milk-allergen. Based on FDA recall #F-0797-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0797-2022%22&limit=1).
Lyons Magnus, Inc. voluntarily recalled Dunkin Caramel Swirl Syrup due to an undeclared milk allergen, the FDA said on Jan. 26, 2022. The Food and Drug Administration announced the Class I recall of 1,900 cases distributed initially to Arizona.
How to tell if you have it
Brand: Lyons Magnus
Product: Dunkin Caramel Swirl Syrup
Product number: 4862
UPC case: 10045796048628
Batch code: 6002
Use by date: 05/Jul 2022
Military time stamp: Included on individual containers
The hazard
The product contains undeclared milk because the individual containers inside the case are incorrectly labeled as Dunkin Mocha Swirl, which does not declare milk as an allergen. The ingredients for the actual Caramel Swirl include sweetened condensed nonfat milk.
Context
GovInfoNow's records show Lyons Magnus, Inc. has two other recalls on file since Sept. 27, 2019. On July 22, 2022, the company issued a recall for Kate Farms Peptide Nutrition Formula due to potential Cronobacter sakazakii and Clostridium botulinum hazards. Other recent recalls of similar products include The Better Bakehouse Donutful Donuts (Aug. 17, 2026), Wawa Fruit Punch Pint (April 2, 2026), and Karison ALSI PINNI 12oz (Jan. 6, 2026).
How to tell if you have this one
Look for 6x 64 fl. oz. cases of Dunkin Caramel Swirl with Product number 4862 and UPC case 10045796048628. Check the individual containers inside; if they are labeled as Dunkin Mocha Swirl, check for Batch 6002 and a use-by date of 05/Jul 2022.
Brand
Lyons Magnus
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop consuming the product
Do not eat or drink the syrup if it matches the recalled description, as it contains undeclared milk.
Check your labels and dates
Verify that you have Product number 4862, UPC case 10045796048628, Batch 6002, and a use-by date of 05/Jul 2022.
Contact the manufacturer
Reach out to Lyons Magnus, Inc. for further instructions on disposal or return since no specific remedy is listed in the record.
Where it went and when
Where it was distributed
Distributed in Arizona.
Listed by the agency
Not listed
FDA distribution: “Initial distribution to AZ” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0797-2022 (January 26, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0797-2022 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.