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shanghai xuerong biotechnology co., ltd

FDA import alert and refusal historyShanghai, ChinaFEI 3010881922

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Example subjectshanghai xuerong biotechnology co., lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, shanghai xuerong biotechnology co., ltd (Shanghai, China) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for enoki mushroom; seafood mushroom; xuerong mushroom, published by FDA on January 30, 2023, 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 · POISONOUS
Last warning letter
None found
Last inspection
None on record

Every FDA record for shanghai xuerong biotechnology co., ltd

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

2023

  1. Import refusal
    Refused, EnokitakePOISONOUSMFR INSANMFR INJEntry EQF-0050584-4
    Source
  2. Import refusal
    Refused, Mushrooms and other fungi products, whole (button), n.e.c.LISTERIAEntry AQZ-0554213-2
    Source
  3. Import refusal
    Refused, EnokitakeMFR INSANMFR INJEntry EQF-0050312-0
    Source
  4. Import alert listing
    Listed on Import Alert 99-23red listEnoki Mushroom; Seafood Mushroom; Xuerong Mushroom
    Source

2022

  1. Import refusal
    Refused, Mushrooms and other fungi products, pieces and stems, sliced, n.e.c.POISONOUSEntry EKH-0803821-1
    Source
  2. Import refusal
    Refused, Enokitake mushrooms, whole (button) (fungi)LISTERIAEntry EQF-0045344-1
    Source

Refusal charges, in plain English

  • LISTERIA2 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.

  • MFR INJ2 refused lines

    Insanitary conditions, may be injurious

    The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.

  • MFR INSAN2 refused lines

    Insanitary manufacturing, processing or packing

    The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.

  • POISONOUS2 refused lines

    Poisonous or deleterious substance

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

Questions about shanghai xuerong biotechnology co., ltd

Is shanghai xuerong biotechnology co., ltd on an FDA import alert?
Yes. As of October 26, 2026, shanghai xuerong biotechnology co., ltd is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for enoki mushroom; seafood mushroom; xuerong mushroom; FDA published the listing on January 30, 2023.
Has FDA refused shipments from shanghai xuerong biotechnology co., ltd?
Yes. FDA refused 5 shipment lines from shanghai xuerong biotechnology co., ltd between October 31, 2022 and July 10, 2023. The most recent, on July 10, 2023, was enokitake, charged as POISONOUS (poisonous or deleterious substance).
Why did FDA refuse shanghai xuerong biotechnology co., ltd's shipments?
The most frequent charges are LISTERIA (listeria monocytogenes, 2 lines) and MFR INJ (insanitary conditions, may be injurious, 2 lines).
What is shanghai xuerong biotechnology co., ltd's FEI number?
shanghai xuerong biotechnology co., ltd's FDA Establishment Identifier (FEI) is 3010881922.
Can shipments from shanghai xuerong biotechnology co., ltd still enter the U.S.?
Shipments of enoki mushroom; seafood mushroom; xuerong mushroom from shanghai 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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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.