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Aqualife PK

FDA import alert and refusal historyYamkino, RussiaFEI 3011424588

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As of October 25, 2026, Aqualife PK (Yamkino, Russia) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for tarkhum carbonated soft drink, published by FDA on September 19, 2012, and has 1 FDA import refusal recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Carbonated soft drink, n.e.c. · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Aqualife PK

2 records, newest first. Each line links to the FDA page it came from.

2018

  1. Import refusal
    Refused, Carbonated soft drink, n.e.c.FILTHYEntry KM6-3513137-8
    Source

2012

  1. Import alert listing
    Listed on Import Alert 45-02red listTarkhum Carbonated Soft Drink
    Source

Refusal charges, in plain English

  • FILTHY1 refused line

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about Aqualife PK

Is Aqualife PK on an FDA import alert?
Yes. As of October 25, 2026, Aqualife PK is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for tarkhum carbonated soft drink; FDA published the listing on September 19, 2012.
Has FDA refused shipments from Aqualife PK?
Yes. FDA refused 1 shipment line from Aqualife PK on April 12, 2018. The most recent, on April 12, 2018, was carbonated soft drink, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Aqualife PK's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is Aqualife PK's FEI number?
Aqualife PK's FDA Establishment Identifier (FEI) is 3011424588.
Can shipments from Aqualife PK still enter the U.S.?
Shipments of tarkhum carbonated soft drink from Aqualife PK can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.