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Handyware Philippines, Inc.

FDA import alert and refusal historyQuezon City, PhilippinesFEI 3006996830

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Example subjectHandyware Philippines, Inc added to Import Alert 16-129 (red list)

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As of October 26, 2026, Handyware Philippines, Inc. (Quezon City, Philippines) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for ube flavor drink mix, published by FDA on January 14, 2010, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Handyware Philippines, Inc.

1 record, newest first. Each line links to the FDA page it came from.

2010

  1. Import alert listing
    Listed on Import Alert 45-02red listUbe Flavor Drink Mix
    Source

Questions about Handyware Philippines, Inc.

Is Handyware Philippines, Inc. on an FDA import alert?
Yes. As of October 26, 2026, Handyware Philippines, Inc. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for ube flavor drink mix; FDA published the listing on January 14, 2010.
Has FDA refused shipments from Handyware Philippines, Inc.?
No FDA import refusals for Handyware Philippines, Inc. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Handyware Philippines, Inc.'s FEI number?
Handyware Philippines, Inc.'s FDA Establishment Identifier (FEI) is 3006996830.
Can shipments from Handyware Philippines, Inc. still enter the U.S.?
Shipments of ube flavor drink mix from Handyware Philippines, Inc. 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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Example subjectHandyware Philippines, Inc added to Import Alert 16-129 (red list)

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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.