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FDA import refusals

FDA import refusals: meal replacements from South Africa

FDA category: Dietary Conventional Foods and Meal Replacements · October 2016 to May 2, 2025

FDA refused 5 meal replacements shipment lines from South Africa between October 2016 and May 2, 2025, 4 of them in 2025; the most refused product was dietary conventional foods, most often for UNAPPROVED (unapproved new drug).

Data from FDA public records, last checked .

5
meal replacements lines refused since October 2016
4
refused so far in 2025
0
firms with the most records, listed below

Meal replacements refusals from South Africa by year

Shipment lines FDA refused each year. The table has the same numbers as the chart.
Bar chart: refusal lines by 2022 to 2025. The same numbers are in the table.012342022: 1 refusal lines’222025: 4 refusal lines4’25
Refusal lines by year
YearRefusal linesvs prior year
20254
20221

Dietary conventional foods refusals from South Africa

FDA refused 5 dietary conventional foods lines from South Africa between October 2016 and May 2, 2025, 100% of the meal replacements lines.
Dietary conventional foods product descriptions refused from South Africa
FDA product descriptionLinesShare of meal replacements
Dietary conventional foods, n.e.c.5100.0%

Recent dietary conventional foods refusals

Recent Dietary conventional foods refusals from South Africa
DateFirmProductCharges
VelobioticsGermiston, South AfricaDietary conventional foods, n.e.cUNAPPROVEDSource
VelobioticsGermiston, South AfricaDietary conventional foods, n.e.cUNAPPROVEDSource
VelobioticsGermiston, South AfricaDietary conventional foods, n.e.cUNAPPROVEDSource
VelobioticsGermiston, South AfricaDietary conventional foods, n.e.cUNAPPROVEDSource
Cape Kingdom NutraceuticalsCape Town, South AfricaDietary conventional foods, n.e.cDIETARYLBLLACKS FIRMLABELINGSource

Why FDA refused meal replacements from South Africa

FDA records a charge code on each refused line; one line can carry several.
Most frequent refusal charges for meal replacements from South Africa
Charge codeMeaningLinesShare
UNAPPROVEDUnapproved new drug457%
DIETARYLBLNot identified as a dietary supplement114%
LABELINGFair Packaging and Labeling Act114%
LACKS FIRMManufacturer name and address missing114%

Import alerts for meal replacements that list South Africa firms

Import alerts for meal replacements listing firms in South Africa
AlertCoversRedGreen
41-03Adulterated and Misbranded Medical Foods1

Latest meal replacements refusals from South Africa

Latest FDA meal replacements refusals from South Africa
DateFirmProductCharges
VelobioticsGermiston, South AfricaDietary conventional foods, n.e.cUNAPPROVEDSource
VelobioticsGermiston, South AfricaDietary conventional foods, n.e.cUNAPPROVEDSource
VelobioticsGermiston, South AfricaDietary conventional foods, n.e.cUNAPPROVEDSource
VelobioticsGermiston, South AfricaDietary conventional foods, n.e.cUNAPPROVEDSource
Cape Kingdom NutraceuticalsCape Town, South AfricaDietary conventional foods, n.e.cDIETARYLBLLACKS FIRMLABELINGSource

Questions about meal replacements refusals from South Africa

How many meal replacements shipments from South Africa did FDA refuse in 2025?
FDA refused 4 shipment lines of meal replacements from South Africa in 2025 through May 2, 2025.
Why does FDA refuse meal replacements from South Africa?
FDA records a charge code on every refused shipment line. For meal replacements from South Africa the most frequent are UNAPPROVED (unapproved new drug, 4 lines), DIETARYLBL (not identified as a dietary supplement, 1 line) and LABELING (Fair Packaging and Labeling Act, 1 line). A charge describes what FDA's reference table says about one shipment line, not about every firm.
Which import alerts cover meal replacements from South Africa?
As of October 26, 2026, the FDA import alerts for this category that list South Africa firms are Import Alert 41-03 (1 firm). General food alerts numbered 99-xx can list South Africa firms too; see the country page.

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.