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Guangzhou Xuerong Biotechnology Co., Ltd

FDA import alert and refusal historyHuizhou City, ChinaFEI 3021593777

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Example subjectGuangzhou Xuerong Biotechnology Co., Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Guangzhou Xuerong Biotechnology Co., Ltd (Huizhou City, China) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for enoki mushrooms, published by FDA on March 9, 2022, and has 5 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Enokitake · LISTERIA
Last warning letter
None found
Last inspection
None on record

Every FDA record for Guangzhou Xuerong Biotechnology Co., Ltd

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

2022

  1. Import refusal
    Refused, 3 lines in one entry: EnokitakeLISTERIANO ENGLISHEntry 9RX-0319842-6Show 3 lines
    Source
  2. Import alert listing
    Listed on Import Alert 99-23red listEnoki mushrooms
    Source
  3. Import refusal
    Refused, 2 lines in one entry: Enokitake mushrooms, whole (button) (fungi)NO ENGLISHEntry 9RX-0319808-7Show 2 lines
    • Refused, Enokitake mushrooms, whole (button) (fungi)NO ENGLISHEntry 9RX-0319808-7Source
    • Refused, Enokitake mushrooms, whole (button) (fungi)NO ENGLISHEntry 9RX-0319808-7Source
    Source

Refusal charges, in plain English

  • NO ENGLISH5 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • LISTERIA3 refused lines

    Listeria monocytogenes

    The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

Questions about Guangzhou Xuerong Biotechnology Co., Ltd

Is Guangzhou Xuerong Biotechnology Co., Ltd on an FDA import alert?
Yes. As of October 26, 2026, Guangzhou Xuerong Biotechnology Co., Ltd is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for enoki mushrooms; FDA published the listing on March 9, 2022.
Has FDA refused shipments from Guangzhou Xuerong Biotechnology Co., Ltd?
Yes. FDA refused 5 shipment lines from Guangzhou Xuerong Biotechnology Co., Ltd between February 18, 2022 and March 10, 2022. The most recent, on March 10, 2022, was enokitake, charged as LISTERIA (listeria monocytogenes).
Why did FDA refuse Guangzhou Xuerong Biotechnology Co., Ltd's shipments?
The most frequent charges are NO ENGLISH (required label information not in english, 5 lines) and LISTERIA (listeria monocytogenes, 3 lines).
What is Guangzhou Xuerong Biotechnology Co., Ltd's FEI number?
Guangzhou Xuerong Biotechnology Co., Ltd's FDA Establishment Identifier (FEI) is 3021593777.
Can shipments from Guangzhou Xuerong Biotechnology Co., Ltd still enter the U.S.?
Shipments of enoki mushrooms from Guangzhou Xuerong Biotechnology Co., Ltd can be detained without physical examination under Import Alert 99-23; 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 subjectGuangzhou Xuerong Biotechnology Co., Lt 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.