CLASS I Food recall · Reported 25 Dec 2019 · FDA Enforcement Report

Tainy Vostoka Dry Fruit Mix Quince Compote recalled by Euroline Foods

Euroline Foods is recalling Tainy Vostoka Dry Fruit Mix Quince Compote, distributed in New Jersey, New York, Pennsylvania. The recall was initiated on 3 Sep 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesContainer code# 27032019. Product UPC code is 4605932006203.
Quantity recalled260 pieces (13 cases with 20 pieces each)

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-0343-2020
FDA event ID
84333
Recalling firm
Euroline Foods, Staten Island, NY
Classification
Class I
Status
Terminated
Recall initiated
3 Sep 2019
FDA classified
18 Dec 2019
Reported
25 Dec 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Sulfites
Product category
Fish

Timeline

3 Sep 2019Recall initiated by company
18 Dec 2019Classified by FDA+106 days
25 Dec 2019Published in enforcement report+7 days

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

Reason for recall

DRY FRUIT MIX QUINCE COMPOTE(TAINY VOSTOKA) contains undeclared sulfites

Product as listed by the FDA

TAINY VOSTOKA DRY FRUIT MIX QUINCE COMPOTE 17.65oz (500 gram); Container code# 27032019; UPC code 4605932006203.

Where it was distributed

Retail throughout NY, NJ, and PA

New JerseyNew YorkPennsylvania

Questions about this recall

Why was it recalled?

DRY FRUIT MIX QUINCE COMPOTE(TAINY VOSTOKA) contains undeclared sulfites

Which lots are affected?

Container code# 27032019. Product UPC code is 4605932006203.

Where was it sold?

Retail throughout NY, NJ, and PA

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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