SupplierRadar

Classic Mode Sdn Bhd

FDA import alert and refusal historyKawasan Perindustrian Cheras Jay, MalaysiaFEI 3039306347

Recorded by FDA as CLASSIC MODE SDN BHD

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Example subjectClassic Mode Sdn Bh added to Import Alert 16-129 (red list)

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As of October 26, 2026, Classic Mode Sdn Bhd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 11, 2026, most often for animal drug residue (VETDRUGRES).

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

Current status

Import alerts
Not listed
Last import refusal
Shrimp & prawns · VETDRUGRES
Last warning letter
None found
Last inspection
None on record

Every FDA record for Classic Mode Sdn Bhd

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

2026

  1. Import refusal
    Refused, Shrimp & prawnsVETDRUGRESEntry EJ2-0201582-5
    Source

Refusal charges, in plain English

  • VETDRUGRES1 refused line

    Animal drug residue

    The product appeared to contain a new animal drug, or a conversion product of one, that is unsafe within the meaning of section 512 of the FD&C Act.

Questions about Classic Mode Sdn Bhd

Is Classic Mode Sdn Bhd on an FDA import alert?
No listing for Classic Mode Sdn Bhd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Malaysia page.
Has FDA refused shipments from Classic Mode Sdn Bhd?
Yes. FDA refused 1 shipment line from Classic Mode Sdn Bhd on February 11, 2026. The most recent, on February 11, 2026, was shrimp & prawns, charged as VETDRUGRES (animal drug residue).
Why did FDA refuse Classic Mode Sdn Bhd's shipments?
The most frequent charge is VETDRUGRES (animal drug residue, 1 line).
What is Classic Mode Sdn Bhd's FEI number?
Classic Mode Sdn Bhd's FDA Establishment Identifier (FEI) is 3039306347.

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Example subjectClassic Mode Sdn Bh 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.