CLASS II Food recall · Reported 19 Jul 2017 · FDA Enforcement Report

Dawn's Foods Tropical Fruit Dip recalled by Morski Brands

Morski Brands is recalling Dawn's Foods Tropical Fruit Dip, distributed in Wisconsin. The recall was initiated on 18 May 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesProduction #13638
Quantity recalled80 lbs. (20 containers)

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-2397-2017
FDA event ID
77363
Recalling firm
Morski Brands, Portage, WI
Brand
Dawn's
Classification
Class II
Status
Terminated
Recall initiated
18 May 2017
FDA classified
11 Jul 2017
Reported
19 Jul 2017
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Allergens
Product category
Dips & Spreads

Timeline

18 May 2017Recall initiated by company
11 Jul 2017Classified by FDA+54 days
19 Jul 2017Published 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 yellow #5

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Dawn's Foods Tropical Fruit Dip. Nwt WT. 4 lbs. (1.82Kg) Keep Refrigerated. For Foodservice Use only.

Where it was distributed

WI

Wisconsin

Questions about this recall

Why was it recalled?

undeclared yellow #5

Which lots are affected?

Production #13638

Where was it sold?

WI

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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