Aqualife PK
FDA import alert and refusal historyYamkino, RussiaFEI 3011424588
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
- Import alerts
- IA 45-02 · red list
- 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
2012
- Import alert listingListed on Import Alert 45-02red listTarkhum Carbonated Soft DrinkSource
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.