Altunsa Gida San. Tic. A.S.
FDA import alert and refusal historyGaziantep, TurkeyFEI 3012322376
As of October 26, 2026, Altunsa Gida San. Tic. A.S. (Gaziantep, Turkey) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for altunsa custard powder (vanilla); altunsa whipped cream strawberry (creme chantilly strawberry); altunsa whipped cream cacao (creme chantilly cacao); jelly strawberry flavored; jelly cherry flavored; jelly orange flavored, published by FDA on November 13, 2024, and has 3 FDA import refusals 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
- Icing and icing mixes without chocolate or nuts · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Altunsa Gida San. Tic. A.S.
4 records, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 45-02red listALTUNSA CUSTARD POWDER (Vanilla); ALTUNSA WHIPPED CREAM STRAWBERRY (Creme Chantilly Strawberry); ALTUNSA WHIPPED CREAM CACAO (Creme Chantilly Cacao); Jelly strawberry flavored; Jelly cherry flavored; Jelly orange flavoredSource
- Import refusalSource
Refused, 3 lines in one entry: Icing and icing mixes without chocolate or nuts; Cake prepared dry mix with custard or cream fillingUNSAFE COLLACKS N/CNUTRIT LBLEntry 805-0135757-0Show 3 linesHide lines
- Refused, Icing and icing mixes without chocolate or nutsUNSAFE COLLACKS N/CNUTRIT LBLEntry 805-0135757-0Source
- Refused, Cake prepared dry mix with custard or cream fillingUNSAFE COLLACKS N/CNUTRIT LBLEntry 805-0135757-0Source
- Refused, Icing and icing mixes without chocolate or nutsUNSAFE COLLACKS N/CNUTRIT LBLEntry 805-0135757-0Source
Refusal charges, in plain English
- LACKS N/C3 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 LBL3 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 COL3 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.
Questions about Altunsa Gida San. Tic. A.S.
- Is Altunsa Gida San. Tic. A.S. on an FDA import alert?
- Yes. As of October 26, 2026, Altunsa Gida San. Tic. A.S. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for altunsa custard powder (vanilla); altunsa whipped cream strawberry (creme chantilly strawberry); altunsa whipped cream cacao (creme chantilly cacao); jelly strawberry flavored; jelly cherry flavored; jelly orange flavored; FDA published the listing on November 13, 2024.
- Has FDA refused shipments from Altunsa Gida San. Tic. A.S.?
- Yes. FDA refused 3 shipment lines from Altunsa Gida San. Tic. A.S. on November 1, 2024. The most recent, on November 1, 2024, was icing and icing mixes without chocolate or nuts, charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Altunsa Gida San. Tic. A.S.'s shipments?
- The most frequent charges are LACKS N/C (net quantity statement missing, 3 lines) and NUTRIT LBL (nutrition information missing from label, 3 lines).
- What is Altunsa Gida San. Tic. A.S.'s FEI number?
- Altunsa Gida San. Tic. A.S.'s FDA Establishment Identifier (FEI) is 3012322376.
- Can shipments from Altunsa Gida San. Tic. A.S. still enter the U.S.?
- Shipments of altunsa custard powder (vanilla); altunsa whipped cream strawberry (creme chantilly strawberry); altunsa whipped cream cacao (creme chantilly cacao); jelly strawberry flavored; jelly cherry flavored; jelly orange flavored from Altunsa Gida San. Tic. A.S. 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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