CLASS I Food recall · Reported 19 Feb 2020 · FDA Enforcement Report

DaVinci Gourmet, Classic Caramel Flavored Sauce, in plastic jugs recalled

Kerry is recalling DaVinci Gourmet, Classic Caramel Flavored Sauce, in plastic jugs, distributed in Arkansas, Colorado, Texas. The recall was initiated on 20 Nov 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC code: 7-37384-06401-3, Enjoy by Date: 28 AUG 2020, Lot number: 0829950901
Quantity recalled100 1 gal jugs

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0684-2020
FDA event ID
84348
Recalling firm
Kerry, Beloit, WI
Brand
DaVinci
Classification
Class I
Status
Terminated
Recall initiated
20 Nov 2019
FDA classified
11 Feb 2020
Reported
19 Feb 2020
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Milk
Product category
Sauces & Condiments

Timeline

20 Nov 2019Recall initiated by company
11 Feb 2020Classified by FDA+83 days
19 Feb 2020Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared milk allergen due to an incorrect back label being placed on the product.

Product as listed by the FDA

DaVinci Gourmet, Classic Caramel Flavored Sauce, 128 FL OZ (1 GAL), in plastic jugs

Where it was distributed

Firm distributed this product to 3 customers located in CO, TX, and AR

ArkansasColoradoTexas

Questions about this recall

Why was it recalled?

Undeclared milk allergen due to an incorrect back label being placed on the product.

Which lots are affected?

UPC code: 7-37384-06401-3, Enjoy by Date: 28 AUG 2020, Lot number: 0829950901

Where was it sold?

Firm distributed this product to 3 customers located in CO, TX, and AR

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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