SAD, Division of Pioneer Foods LTD
FDA import alert and refusal historyWellington, South AfricaFEI 3004261061
As of October 27, 2026, SAD, Division of Pioneer Foods LTD (Wellington, South Africa) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for safari fruit dianty cube, published by FDA on September 9, 2010, is also listed on Import Alert 99-21 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red listIA 99-21 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for SAD, Division of Pioneer Foods LTD
2 records, newest first. Each line links to the FDA page it came from.
2010
- Import alert listingListed on Import Alert 45-02red listSafari Fruit Dianty CubeSource
2009
- Import alert listingListed on Import Alert 99-21red listRaisins (Dried Grapes) (Berry); Raisins, Dried or PasteSource
Questions about SAD, Division of Pioneer Foods LTD
- Is SAD, Division of Pioneer Foods LTD on an FDA import alert?
- Yes. As of October 27, 2026, SAD, Division of Pioneer Foods LTD is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for safari fruit dianty cube; FDA published the listing on September 9, 2010.
- Has FDA refused shipments from SAD, Division of Pioneer Foods LTD?
- No FDA import refusals for SAD, Division of Pioneer Foods LTD appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is SAD, Division of Pioneer Foods LTD's FEI number?
- SAD, Division of Pioneer Foods LTD's FDA Establishment Identifier (FEI) is 3004261061.
- Can shipments from SAD, Division of Pioneer Foods LTD still enter the U.S.?
- Shipments of safari fruit dianty cube from SAD, Division of Pioneer Foods LTD can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.