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FDA Detention Sampling & Testing Services

Product & Industry Guide

FDA Detention Testing for Spices & Seasonings

Imported spices are frequently detained for Salmonella, illegal dyes, filth, and mycotoxins. Here's why FDA holds spice shipments, which import alerts apply, and what sampling and testing typically involve.

Imported spices and seasonings at an inspection facility subject to FDA detention testing

The Short Version

Why Spice Shipments Get Detained

Spices and seasonings are among the most Salmonella-detained foods, and they also face illegal-color and filth charges. Because spices are often grown, dried, and handled in open-air conditions, contamination with Salmonella or filth is common, and some suppliers illegally add unapproved dyes — like Sudan colors in chili and paprika — to enhance appearance. Certain spices also carry mycotoxin risk. Each charge demands a different test, so identifying exactly what FDA cited is the first step.

The Common Charges

What Spices Get Charged For

Salmonella
The leading spice detention. A zero-tolerance pathogen charge — presence in a representative sample renders the spice adulterated.
Illegal Dyes
Non-permitted colors such as Sudan I-IV, para red, or Rhodamine B added to chili, paprika, turmeric, or curry blends to boost color — an adulteration charge that relabeling cannot fix.
Filth
Insect fragments, rodent hair, or other filth detected on inspection — common in bulk, open-dried spices.
Mycotoxins
Aflatoxins and ochratoxin in certain spices (e.g., chili, nutmeg, paprika), tied to storage and humidity.
Undeclared Colors
Even a permitted color not declared on the label is a misbranding charge — sometimes correctable, unlike a non-permitted dye.
Heavy Metals
Lead and other metals appear in some spices, occasionally from adulteration or environmental sources.

The Testing

What Spice Testing Involves

  1. Representative Sampling

    A trained sampler collects representative sub-samples across the lot under documented custody — important for spices, where contamination like Salmonella or aflatoxin is often unevenly distributed.

  2. Analyte-Matched Analysis

    The charge dictates the method: microbiological culture for Salmonella, chromatographic dye analysis for illegal colors, LC-MS/MS or ELISA for mycotoxins, at an appropriately accredited (often LAAF) lab.

  3. Package & Submit

    Results, methods, and custody records are assembled into an analytical package and submitted to FDA, typically via ITACS, for review. FDA makes the final admissibility decision.

Uneven contamination makes sampling design critical. With spices, where you sample matters as much as how you test. See how sampling is documented in our chain of custody guide.

Be Realistic

Honest Notes on Spice Detentions

Set expectations honestly

  • An illegal dye can't be declared away. If a non-permitted color like a Sudan dye is present, the spice is adulterated regardless of labeling — testing confirms rather than clears it.
  • Zero-tolerance means zero. For Salmonella, a positive in a representative sample is disqualifying; testing shows a clean sample but can't remove a pathogen that's present.
  • Sampling design can make or break the case. Uneven contamination means a poorly designed sample can produce a misleading result and a rejected package.
  • Release isn't removal. Clearing one spice shipment doesn't lift an alert on the firm or country; that's a separate removal petition.
  • No guaranteed outcome. We coordinate defensible sampling and testing to give your evidence its best footing — but FDA decides admissibility.

Spices Detained?

Send the Notice — We'll Match the Right Test

Send your Notice of FDA Action and the spice or blend involved. You'll get a quick, honest read on whether the charge points to Salmonella, an illegal dye, mycotoxins, or filth — and what testing can do.

Urgent detention matters receive priority intake review.

FDA Detention Sampling is an independent private company. We are not affiliated with, endorsed by, or part of the U.S. Food and Drug Administration. This guide is general information about FDA import detention and testing for spices and seasonings; the charge and instructions on your specific Notice of FDA Action, and the applicable import alert, control. Sampling, laboratory testing, documentation, and coordination services do not guarantee FDA release, admissibility, acceptance of laboratory results, removal from any import alert, or any specific regulatory outcome. FDA makes the final admissibility decision.