Oman Refreshment Company
FDA import alert and refusal historyBowsher, OmanFEI 3025812467
Recorded by FDA as OMAN REFRESHMENT COMPANY
As of October 25, 2026, Oman Refreshment Company (Bowsher, Oman) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for miranda soda (glass); miranda soda (can); mountain dew soda (can); mountain dew soda (glass), published by FDA on December 13, 2024, is also listed on Import Alert 45-02 (red list), and has 4 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red listIA 45-02 · red list
- Last import refusal
- Soft drink, cola, carbonated · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Oman Refreshment Company
6 records, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 99-39red listMiranda Soda (Glass); Miranda Soda (Can); Mountain Dew Soda (Can); Mountain Dew Soda (Glass)Source
- Import alert listingListed on Import Alert 45-02red listMiranda Soda; Mountain Dew SodaSource
- Import refusalSource
Refused, 4 lines in one entry: Soft drink, cola, carbonatedUNSAFE COLCOLOR LBLGLACKS N/CNUTRIT LBLEntry 8V6-0036668-7Show 4 linesHide lines
- Refused, Soft drink, cola, carbonatedUNSAFE COLCOLOR LBLGLACKS N/CNUTRIT LBLEntry 8V6-0036668-7Source
- Refused, Soft drink, cola, carbonatedUNSAFE COLCOLOR LBLGLACKS N/CNO ENGLISHNUTRIT LBLEntry 8V6-0036668-7Source
- Refused, Soft drink, cola, carbonatedUNSAFE COLCOLOR LBLGLACKS N/CNO ENGLISHNUTRIT LBLEntry 8V6-0036668-7Source
- Refused, Soft drink, cola, carbonatedUNSAFE COLCOLOR LBLGLACKS N/CNUTRIT LBLEntry 8V6-0036668-7Source
Refusal charges, in plain English
- COLOR LBLG4 refused lines
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- LACKS N/C4 refused lines
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- NUTRIT LBL4 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- UNSAFE COL4 refused lines
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
- NO ENGLISH2 refused lines
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
Questions about Oman Refreshment Company
- Is Oman Refreshment Company on an FDA import alert?
- Yes. As of October 25, 2026, Oman Refreshment Company is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for miranda soda (glass); miranda soda (can); mountain dew soda (can); mountain dew soda (glass); FDA published the listing on December 13, 2024.
- Has FDA refused shipments from Oman Refreshment Company?
- Yes. FDA refused 4 shipment lines from Oman Refreshment Company on September 4, 2024. The most recent, on September 4, 2024, was soft drink, cola, carbonated, charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Oman Refreshment Company's shipments?
- The most frequent charges are COLOR LBLG (artificial coloring not declared, 4 lines) and LACKS N/C (net quantity statement missing, 4 lines).
- What is Oman Refreshment Company's FEI number?
- Oman Refreshment Company's FDA Establishment Identifier (FEI) is 3025812467.
- Can shipments from Oman Refreshment Company still enter the U.S.?
- Shipments of miranda soda (glass); miranda soda (can); mountain dew soda (can); mountain dew soda (glass) from Oman Refreshment Company can be detained without physical examination under Import Alert 99-39; 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.