Euroline Foods Tainy Vostoka Quince Compote Recall: Undeclared Sulfites
Euroline Foods recalls Tainy Vostoka Quince Compote due to undeclared sulfites. Consumers should check product codes to determine if affected.
Lower-risk recall
DRY FRUIT MIX QUINCE COMPOTE(TAINY VOSTOKA) contains undeclared sulfites
Contact the company
What happened, in plain English
Euroline Foods is recalling Tainy Vostoka Quince Compote because it contains undeclared sulfites. This could cause allergic reactions in people sensitive to sulfites. Read more at govinfonow.com/recall/16687-euroline-foods-tainy-vostoka-quince-compote-recall-undeclared-sulfites.
Source Summary by GovInfoNow · govinfonow.com/recall/16687-euroline-foods-tainy-vostoka-quince-compote-recall-undeclared-sulfites · Updated October 5, 2026 · FDA enforcement record: FDA #F-0343-2020
Cite this page
“Euroline Foods Tainy Vostoka Quince Compote Recall: Undeclared Sulfites.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16687-euroline-foods-tainy-vostoka-quince-compote-recall-undeclared-sulfites. Based on FDA recall #F-0343-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0343-2020%22&limit=1).
Why it’s dangerous
Sulfites are preservatives that can cause allergic reactions in sensitive individuals. The product contains sulfites without being declared on the label.
Who’s affected
People who purchased the Tainy Vostoka Quince Compote from Euroline Foods. Those with sulfite allergies are at higher risk.
How to tell if you have this one
Check for container code #27032019 or UPC code 4605932006203 on the product label.
- Brand
Euroline Foods- Product
TAINY VOSTOKA DRY FRUIT MIX QUINCE COMPOTE 17.65oz (500 gram); Container code# 27032019; UPC code 4605932006203- Category
Food
What to do — step by step
Check Product Label
Look for container code #27032019 or UPC code 4605932006203 to identify affected items.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “Retail throughout NY, NJ, and PA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New Jersey, New York, Pennsylvania.
Recall timeline
FDA terminated this recall 4 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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-0343-2020 (September 3, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0343-2020 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.