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Dr Foerster (M) Sdn Bhd

FDA import alert and refusal historyShah Alam, MalaysiaFEI 3014215045

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Example subjectDr Foerster (M) Sdn Bh added to Import Alert 16-129 (red list)

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As of October 26, 2026, Dr Foerster (M) Sdn Bhd (Shah Alam, Malaysia) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for dr foerster detox plus food supplement; ultra detox capsules, published by FDA on November 27, 2018, and has 2 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · UNSFDIETSP
Last warning letter
None found
Last inspection
None on record

Every FDA record for Dr Foerster (M) Sdn Bhd

3 records, newest first. Each line links to the FDA page it came from.

2019

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNSFDIETSPUNSAFE ADDPOISONOUSEntry 799-3440036-5
    Source
  2. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 799-3447557-3
    Source

2018

  1. Import alert listing
    Listed on Import Alert 54-16red listDr Foerster Detox Plus Food Supplement; Ultra Detox Capsules
    Source

Refusal charges, in plain English

  • POISONOUS1 refused line

    Poisonous or deleterious substance

    The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.

  • UNAPPROVED1 refused line

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

  • UNSAFE ADD1 refused line

    Food additive unsafe under section 409

    The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

  • UNSFDIETSP1 refused line

    Dietary ingredient without safety assurance

    The product appeared to be a dietary supplement or dietary ingredient for which there is inadequate information to provide reasonable assurance that it does not present a significant or unreasonable risk of illness or injury.

Questions about Dr Foerster (M) Sdn Bhd

Is Dr Foerster (M) Sdn Bhd on an FDA import alert?
Yes. As of October 26, 2026, Dr Foerster (M) Sdn Bhd is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for dr foerster detox plus food supplement; ultra detox capsules; FDA published the listing on November 27, 2018.
Has FDA refused shipments from Dr Foerster (M) Sdn Bhd?
Yes. FDA refused 2 shipment lines from Dr Foerster (M) Sdn Bhd between November 21, 2019 and December 2, 2019. The most recent, on December 2, 2019, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as UNSFDIETSP (dietary ingredient without safety assurance).
Why did FDA refuse Dr Foerster (M) Sdn Bhd's shipments?
The most frequent charges are POISONOUS (poisonous or deleterious substance, 1 line) and UNAPPROVED (unapproved new drug, 1 line).
What is Dr Foerster (M) Sdn Bhd's FEI number?
Dr Foerster (M) Sdn Bhd's FDA Establishment Identifier (FEI) is 3014215045.
Can shipments from Dr Foerster (M) Sdn Bhd still enter the U.S.?
Shipments of dr foerster detox plus food supplement; ultra detox capsules from Dr Foerster (M) Sdn Bhd can be detained without physical examination under Import Alert 54-16; 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 subjectDr Foerster (M) 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.