Reference Source

ARUNALU PRODUCTS · 99-39 · SRI LANKA

For ARUNALU PRODUCTS · 99-39 · SRI LANKA, import alert is 99-39; import alert name is Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded; country is SRI LANKA; product is Arunalu Dry Fish Headless Sprats; product code is 16 A - - 01 Anchovy; date published is 06/13/2016; address is Kandawala , 30/7 Torington Estate , Katana, Gampaha SRI LANKA, verified against its source on 2026-09-16.

Firm
ARUNALU PRODUCTS verified
Import alert
99-39
Import alert name
Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded
Country
SRI LANKA verified
Address
Kandawala , 30/7 Torington Estate , Katana, Gampaha SRI LANKA verified
Date published
06/13/2016 verified
Product code
16 A - - 01 Anchovy verified
Product
Arunalu Dry Fish Headless Sprats verified
FDA notes
The article is subject to refusal of admission pursuant to Section 801(a)(3) for the following: It appears to be misbranded within the meaning of section 403(q) of the Act [21 U.S.C. § 343(q)] in that the nutrition information is not in an appropriate format as defined by 21 CFR 101.9. • The label fails to declare the nutrient information on the correct serving size based on the appropriate reference amount customarily consumed (RACC) in accordance with 21 CFR 10 1.9(b) and 21 CFR 101.12. • The Nutrition Facts label fails to list all the required n nutrients as provided under 21 CFR 101.9(c). It appears to be misbranded within the meaning of Section 403(f) of the Act [21 U.S.C. § 343(f)] in that the product label contains information in two languages but does not repeat all the required label information in both languages. In accordance with 21 CFR 101.15( c )(2), if the label contains any representation in a foreign language, all words, statements, and other information required by or under the authority of the act must appear in the foreign language. It appears to be misbranded within the meaning of section 403(i)(1) of the Act [21 U.S.C. § 343(i)(1)]because the statement of identity on the Principal Display Panel does not accurately describe the product, as required under 21 CFR 101.3. It it appears to be misbranded within the meaning of section 403(i)(2) of the Act [21 U.S.C. § 343(i)(2)] because the label fails to declare the common or usual name of each ingredient, as required under 21 CFR 101.4. verified
Sourceaccessdata.fda.gov
Verified
Review by
DatasetFDA import alert red lists: firms subject to detention without physical examination

What the source says

ARUNALU PRODUCTS Date Published : 06/13/2016 Kandawala , 30/7 Torington Estate , Katana, Gampaha SRI LANKA 16 A - - 01 Anchovy Date Published: 06/13/2016 Desc: Arunalu Dry Fish Headless Sprats Notes: The article is subject to refusal of admission pursuant to Section 801(a)(3) for the following: It appears to be misbranded within the meaning of section 403(q) of the Act [21 U.S.C. § 343(q)] in that the nutrition information is not in an appropriate format as defined by 21 CFR 101.9. • The label fails to declare the nutrient information on the correct serving size based on the appropriate reference amount customarily consumed (RACC) in accordance with 21 CFR 10 1.9(b) and 21 CFR 101.12. • The Nutrition Facts label fails to list all the required n nutrients as provided under 21 CFR 101.9(c). It appears to be misbranded within the meaning of Section 403(f) of the Act [21 U.S.C. § 343(f)] in that the product label contains information in two languages but does not repeat all the required label information in both languages. In accordance with 21 CFR 101.15( c )(2), if the label contains any representation in a foreign language, all words, statements, and other information required by or under the authority of the act must appear in the foreign language. It appears to be misbranded within the meaning of section 403(i)(1) of the Act [21 U.S.C. § 343(i)(1)]because the statement of identity on the Principal Display Panel does not accurately describe the product, as required under 21 CFR 101.3. It it appears to be misbranded within the meaning of section 403(i)(2) of the Act [21 U.S.C. § 343(i)(2)] because the label fails to declare the common or usual name of each ingredient, as required under 21 CFR 101.4.

accessdata.fda.gov, retrieved 2026-09-15

Source

Last verified against source: . Due for re-check by . This page as Markdown · OKF bundle · full dataset as JSON.

This one changes, and we watch it.FDA import alert red lists: firms subject to detention without physical examination is re-read on a schedule and every change is dated. Subscribe: Atom feed · JSON · what has changed so far.