Kerry recalls 128 fl oz caramel sauce due to undeclared milk allergen on back label. Consumers should check UPC 7-37384-06401-3 and lot number 0829950901 for affected products.
“Kerry DaVinci Gourmet Caramel Sauce Recall: Undeclared Milk Allergen.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16251-kerry-davinci-gourmet-caramel-sauce-recall-undeclared-milk-allergen. Based on FDA recall #F-0684-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0684-2020%22&limit=1).
The FDA announced on Nov. 20, 2019, that Kerry, Inc. voluntarily recalled DaVinci Gourmet Classic Caramel Flavored Sauce due to an undeclared milk allergen. The firm distributed the product to customers in Colorado, Texas, and Arkansas.
How to tell if you have it
DaVinci Gourmet, Classic Caramel Flavored Sauce, 128 FL OZ (1 GAL), in plastic jugs
UPC: 7-37384-06401-3
Enjoy by Date: 28 AUG 2020
Lot number: 0829950901
The hazard
The product carries an incorrect back label, resulting in the undeclared milk allergen. The FDA classified this as a Class I recall.
Context
GovInfoNow's records show Kerry, Inc has issued 7 other recalls since July 11, 2016. Recent Kerry recalls include an egg allergen risk in KC Everyday Mac & Cheese on July 29, 2026, and potential salmonella contamination in Salt & Vinegar 50lb Product on May 3, 2024. Other recent recalls of similar products include Loard's Sea Salt Caramel Ice Cream Recall (April 15, 2026), Wawa Diet Lemonade P Undeclared Milk Allergen Recall (April 2, 2026), and The Better Bakehouse Donutful Donuts Due to Undeclared Milk (Aug. 17, 2026).
How to tell if you have this one
Check for the UPC code 7-37384-06401-3 and lot number 0829950901 on the product. The sauce was sold in 128 fl oz plastic jugs with an enjoy-by date of August 28, 2020.
Brand
Kerry
Product
DaVinci Gourmet, Classic Caramel Flavored Sauce, 128 FL OZ (1 GAL), in plastic jugs
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC code 7-37384-06401-3 and lot number 0829950901 on the sauce container.
Where it went and when
Where it was distributed
Distributed in 3 states.
Listed by the agency
Not listed
FDA distribution: “Firm distributed this product to 3 customers located in CO, TX, and AR” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arkansas, Colorado, Texas.
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-0684-2020 (November 20, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0684-2020 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 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.