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CriticalFDAfda-F-2155-2019UNDECLARED ALLERGEN

TAINY VOSTOKA ASSORTED DRIED FRUITS -APPLE were distributed nationwide in retail stores and through mail orders. The product comes in 50...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
800
Recall Date
August 23, 2019
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2155-2019.

Product contains undeclared sulfites.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2155-2019.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Krasnyi Oktyabr Inc. Usa or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2155-2019.

Krasnyi Oktyabr Inc. USA

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Krasnyi Oktyabr Inc. Usa Recall FAQ

Krasnyi Oktyabr Inc. Usa is the subject of a produce safety report: TAINY VOSTOKA ASSORTED DRIED FRUITS -APPLE were distributed nationwide in retail stores and through mail orders. The product comes in 50.... The notice was published on August 23, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 800 units are potentially affected.