Labelling in US Food Imports — FDA Import Refusals

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Labelling appeared in 7,617 FDA import refusals between 2020 and 2026 — 28.7% of all 26,528 US import refusals. The charge is a labelling or registration failure, not a hazard found in the product. The origins cited most often are Mexico, India, China. The most-affected product category is Vitamins, Minerals, Proteins, and Unconventional Dietary Specialties for Humans. Volume in 2025 was up 21% on 2024.

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Labelling refusals by year

YearRefusalsYoY
2020 802 —
2021 792 -1.2%
2022 942 +18.9%
2023 1,060 +12.5%
2024 1,268 +19.6%
2025 1,538 +21.3%
2026 1,215 — YTD
Total7,617

Origins most cited for Labelling

#Origin countryRefusals
1 Mexico 1,712
2 India 749
3 China 600
4 Canada 296
5 United Kingdom 225
6 Philippines 218
7 South Korea 193
8 Turkey 188
9 Japan 180
10 Guatemala 173
11 Vietnam 154
12 Portugal 140
13 Italy 139
14 Germany 115
15 United States 114
16 Thailand 105
17 Indonesia 102
18 Nigeria 102
19 Switzerland 101
20 Taiwan 93
21 Colombia 89
22 Honduras 85
23 Brazil 79
24 Pakistan 76
25 Spain 67
26 Sweden 63
27 Jordan 59
28 Malaysia 58
29 Bangladesh 54
30 Ghana 53

Product categories where Labelling appears

#Product categoryRefusals
1Vitamins, Minerals, Proteins, and Unconventional Dietary Specialties for Humans1,425
2Snack Food Items (Flour, Meal, or Vegetable Base)995
3Candy Without Chocolate, Candy Specialties, and Chewing Gum608
4Fruit and Fruit Products558
5Bakery Products, Doughs, Bakery Mixes, and Icings489
6Soft Drinks and Waters378
7Vegetables and Vegetable Products360
8Fishery/Seafood Products355
9Dietary Conventional Foods and Meal Replacements278
10Baby (Infant and Junior) Food Products270
11Macaroni and Noodle Products254
12Multiple Food Dinners, Gravies, Sauces, and Specialties (Total Diet)248
13Spices, Flavors, and Salts209
14Chocolate and Cocoa Products145
15Nuts and Edible Seeds144

FDA charge codes in Labelling

CodeWhat it meansRefusals
NUTRIT LBLnutrition labeling3,041
COLOR LBLGcolor not declared2,161
NO ENGLISHnot in English2,101
LIST INGREingredients not listed1,621
LACKS N/Cno net quantity1,442
FALSEfalse or misleading label957
LACKS FIRMno manufacturer name920
LABELINGlabeling751
INCONSPICUlabel not conspicuous678
USUAL NAMEno common name672
DIETARYLBLsupplement labeling353
NCONTACTno contact information286
HEALTH Cunauthorized health claim190
STD IDENTnot to standard of identity133
SULFITELBLsulfites not declared108
COLORLABELcolor additive labeling104
JUICE %juice percentage not declared100
DIRSEXMPTno adequate directions88
DIETARYINGdietary ingredient labeling78
PRESRV LBLpreservative not declared60
FLAVR LBLGflavor not declared55
STD NAMEno standard name54
PLANT PARTplant part not declared44

Recent Labelling refusals

About Labelling

Labelling charges are misbranding findings under FD&C Act Section 403: the product was not necessarily unsafe, but its label omitted or misstated something the law requires — net quantity of contents, the common or usual name, a full ingredient list, required English-language text, nutrition or dietary-supplement information, or conformity with a standard of identity. These findings turn up across nearly every packaged food category, from spices and confectionery to dietary supplements and infant formula, wherever a shipment's paperwork trails its contents.

Which FDA import refusals does this page count?

Every entry FDA refused that cites this hazard among its charge codes. A single entry can carry more than one charge, so an entry refused for both a pathogen and a labelling defect is counted on both the relevant hazard page and, separately, in the hazard/paperwork split shown on the leaderboard.

What happens when this hazard is found in a shipment?

The entry is refused admission into US commerce. The importer must recondition the shipment (where that is possible), export it out of the United States, or have it destroyed under FDA supervision. Repeated findings against one shipper or product can lead FDA to place them on an Import Alert, which subjects future shipments to detention without physical examination.

Where does this data come from?

The public FDA Import Refusal Report, refetched weekly. Counts are per entry (consignment), so one entry listing several charge codes for the same hazard is counted once.