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
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
- Brand
- Tainy Vostoka
- 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 2019 | Recall initiated by company | |
| 18 Dec 2019 | Classified by FDA | +106 days |
| 25 Dec 2019 | Published 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
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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