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Shen Zhen Evergreen Bio-Health Technology

FDA import alert and refusal historyShenzhen, ChinaFEI 3027386235

Recorded by FDA as SHEN ZHEN EVERGREEN BIO-HEALTH TECHNOLOGY

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Example subjectShen Zhen Evergreen Bio-Health Technolog added to Import Alert 16-129 (red list)

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As of October 26, 2026, Shen Zhen Evergreen Bio-Health Technology (Shenzhen, China) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for chlorella powder 8 oz dietary supplement; chlorella 1000 tablets (250g) dietary supplement, published by FDA on September 12, 2024, and has 7 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Dietary conventional foods, n.e.c. · FALSE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Shen Zhen Evergreen Bio-Health Technology

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

2025

  1. Import refusal
    Refused, 7 lines in one entry: Dietary conventional foods, n.e.c.FALSEDIETARYINGNCONTACTNUTRIT LBLEntry INL-0719517-2Show 7 lines
    Source

2024

  1. Import alert listing
    Listed on Import Alert 99-39red listChlorella Powder 8 oz dietary supplement; Chlorella 1000 Tablets (250g) dietary supplement
    Source

Refusal charges, in plain English

  • HEALTH C7 refused lines

    Unauthorized nutrient content or health claim

    The label or labeling appeared to carry a nutrient content claim or health claim that is not authorized.

  • NCONTACT7 refused lines

    No U.S. adverse event contact on supplement label

    The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

  • NUTRIT LBL7 refused lines

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • FALSE6 refused lines

    False or misleading labeling

    The labeling appeared to be false or misleading in some particular.

  • DIETARYLBL5 refused lines

    Not identified as a dietary supplement

    The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).

  • DIETARYING1 refused line

    Dietary ingredients not listed

    The dietary supplement label appeared not to list each dietary ingredient and its quantity, or the total quantity of a proprietary blend.

  • FLAVR LBLG1 refused line

    FLAVR LBLG

Questions about Shen Zhen Evergreen Bio-Health Technology

Is Shen Zhen Evergreen Bio-Health Technology on an FDA import alert?
Yes. As of October 26, 2026, Shen Zhen Evergreen Bio-Health Technology is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for chlorella powder 8 oz dietary supplement; chlorella 1000 tablets (250g) dietary supplement; FDA published the listing on September 12, 2024.
Has FDA refused shipments from Shen Zhen Evergreen Bio-Health Technology?
Yes. FDA refused 7 shipment lines from Shen Zhen Evergreen Bio-Health Technology on January 8, 2025. The most recent, on January 8, 2025, was dietary conventional foods, n.e.c., charged as FALSE (false or misleading labeling).
Why did FDA refuse Shen Zhen Evergreen Bio-Health Technology's shipments?
The most frequent charges are HEALTH C (unauthorized nutrient content or health claim, 7 lines) and NCONTACT (no u.s. adverse event contact on supplement label, 7 lines).
What is Shen Zhen Evergreen Bio-Health Technology's FEI number?
Shen Zhen Evergreen Bio-Health Technology's FDA Establishment Identifier (FEI) is 3027386235.
Can shipments from Shen Zhen Evergreen Bio-Health Technology still enter the U.S.?
Shipments of chlorella powder 8 oz dietary supplement; chlorella 1000 tablets (250g) dietary supplement from Shen Zhen Evergreen Bio-Health Technology can be detained without physical examination under Import Alert 99-39; 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.