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Violation Code: 2680

FDA Violation

Charge Code: SACCHARLBL

366
Total Refusals
131
Affected Firms
9/5/2014
Latest Case
2/4/2002
First Case

Violation Details

Violation Code (ASC ID)
2680
Charge Code
SACCHARLBL
Description
The article contains Saccharin, a non-nutritive sweetener, and its label or labeling fails to list it as an added ingredient
Legal Section
403(i); 803(a)(3) Misbranding

Most Affected Firms

Recent Import Refusals

DateProductFirm
9/5/2014
OLIVES, DRIED OR PASTE
21HGH09
5/1/2014
PLUM, DRIED OR PASTE
21HGT14
4/1/2014
PLUM, DRIED OR PASTE
21HGH14
3/11/2014
OLIVES, DRIED OR PASTE
21HGT09
3/7/2014
PLUM, DRIED OR PASTE
21HGH14
3/4/2014
PLUM, DRIED OR PASTE
21HGH14
3/4/2014
PLUM, DRIED OR PASTE
21HGH14
2/26/2014
FRUIT COCKTAIL, DRIED OR PASTE
21BGH01
2/10/2014
PLUM, DRIED OR PASTE
21HGH14
1/30/2014
LONGAN, DRIED OR PASTE
21TGH18
1/30/2014
LONGAN, DRIED OR PASTE
21TGH18
1/2/2014
RAISINS, DRIED OR PASTE
20BHT10
1/2/2014
OLIVES, DRIED OR PASTE
21HCH09
12/24/2013
FRUITS USED AS VEGETABLES, N.E.C.
24FHE99
12/13/2013
PLUM (PIT FRUIT)
21GGH14

Frequently Asked Questions

What is FDA violation code 2680?

2680 is an FDA violation code that indicates: "The article contains Saccharin, a non-nutritive sweetener, and its label or labeling fails to list it as an added ingredient". This violation is based on 403(i); 803(a)(3) Misbranding of the Federal Food, Drug, and Cosmetic Act.

How many import refusals have been issued for violation 2680?

According to FDA Import Refusal data, there have been 366 import refusals issued for violation code 2680, affecting 131 unique firms.

When was the most recent refusal for violation 2680?

The most recent import refusal for violation 2680 was on September 5, 2014.

What products are commonly refused for violation 2680?

Products commonly refused under violation 2680 include: OLIVES, DRIED OR PASTE, PLUM, DRIED OR PASTE. These products were refused entry because they did not meet FDA requirements.

What is the legal basis for FDA violation code 2680?

Violation code 2680 is based on 403(i); 803(a)(3) Misbranding of the Federal Food, Drug, and Cosmetic Act (FD&C Act). This section of the law establishes requirements that imported products must meet to be allowed entry into the United States.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.