Reference Source

H&A HOLLAND · 99-39 · NETHERLANDS

For H&A HOLLAND · 99-39 · NETHERLANDS, import alert is 99-39; import alert name is Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded; country is NETHERLANDS; product is MAZI TAHIN (SESAME PASTE) | MAZI TAHIN (SESAME PASTE); product code is 23 R - - 02 Sesame Seed (Edible Seed Paste) | 37 K - - 21 Sesame Paste; date published is 12/20/2021; address is Stephensonstraat 10 R , Zoetermeer, Zuid-Holland NETHERLANDS, verified against its source on 2026-09-16.

Firm
H&A HOLLAND verified
Import alert
99-39
Import alert name
Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded
Country
NETHERLANDS verified
Address
Stephensonstraat 10 R , Zoetermeer, Zuid-Holland NETHERLANDS verified
Date published
12/20/2021 verified
Product code
23 R - - 02 Sesame Seed (Edible Seed Paste) | 37 K - - 21 Sesame Paste each item verified
Product
MAZI TAHIN (SESAME PASTE) | MAZI TAHIN (SESAME PASTE) each item verified
FDA notes
The article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that 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 (i.e., Nutrition Facts label, or NFL) fails to comply with the requirements of 21 CFR 101.9. Section 403(f) of the Act [21 U.S.C. §343(f)] because the product label contains information in multiple languages but does not repeat all the required information in all languages. Section 403(e)(2) of the Act [21 U.S.C. §343(e)(2)] because the label’s net quantity of contents statement fails to comply with 21 CFR 101.7. | The article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that 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 (i.e., Nutrition Facts label, or NFL) fails to comply with the requirements of 21 CFR 101.9. Section 403(f) of the Act [21 U.S.C. §343(f)] because the product label contains information in multiple languages but does not repeat all the required information in all languages. Section 403(e)(2) of the Act [21 U.S.C. §343(e)(2)] because the label’s net quantity of contents statement fails to comply with 21 CFR 101.7. each item verified
Sourceaccessdata.fda.gov
Verified
Review by
DatasetFDA import alert red lists: firms subject to detention without physical examination

What the source says

H&A HOLLAND Date Published : 12/20/2021 Stephensonstraat 10 R , Zoetermeer, Zuid-Holland NETHERLANDS 23 R - - 02 Sesame Seed (Edible Seed Paste) Date Published: 12/20/2021 Desc: MAZI TAHIN (SESAME PASTE) Notes: The article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that 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 (i.e., Nutrition Facts label, or NFL) fails to comply with the requirements of 21 CFR 101.9. Section 403(f) of the Act [21 U.S.C. §343(f)] because the product label contains information in multiple languages but does not repeat all the required information in all languages. Section 403(e)(2) of the Act [21 U.S.C. §343(e)(2)] because the label’s net quantity of contents statement fails to comply with 21 CFR 101.7. 37 K - - 21 Sesame Paste Date Published: 12/20/2021 Desc: MAZI TAHIN (SESAME PASTE) Notes: The article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that 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 (i.e., Nutrition Facts label, or NFL) fails to comply with the requirements of 21 CFR 101.9. Section 403(f) of the Act [21 U.S.C. §343(f)] because the product label contains information in multiple languages but does not repeat all the required information in all languages. Section 403(e)(2) of the Act [21 U.S.C. §343(e)(2)] because the label’s net quantity of contents statement fails to comply with 21 CFR 101.7.

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

Source

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