Rafhan Best Foods Limited
FDA import alert and refusal historyLahroe, PakistanFEI 3004651980
As of October 26, 2026, Rafhan Best Foods Limited (Lahroe, Pakistan) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for custard powder; strawberry jam; mango gelatin; pineapple gelatin; banana gelatin; strawberry gelatin; raspberry gelatin, published by FDA on September 18, 2009, 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 list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Rafhan Best Foods Limited
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listcustard powder; Strawberry Jam; Mango gelatin; Pineapple gelatin; Banana Gelatin; Strawberry Gelatin; Raspberry GelatinSource
Questions about Rafhan Best Foods Limited
- Is Rafhan Best Foods Limited on an FDA import alert?
- Yes. As of October 26, 2026, Rafhan Best Foods Limited is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for custard powder; strawberry jam; mango gelatin; pineapple gelatin; banana gelatin; strawberry gelatin; raspberry gelatin; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Rafhan Best Foods Limited?
- No FDA import refusals for Rafhan Best Foods Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Rafhan Best Foods Limited's FEI number?
- Rafhan Best Foods Limited's FDA Establishment Identifier (FEI) is 3004651980.
- Can shipments from Rafhan Best Foods Limited still enter the U.S.?
- Shipments of custard powder; strawberry jam; mango gelatin; pineapple gelatin; banana gelatin; strawberry gelatin; raspberry gelatin from Rafhan Best Foods Limited 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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