Shandong Zhongxing Mushroom Technology Co., Ltd
FDA import alert and refusal historyDezhou, ChinaFEI 3026439459
Recorded by FDA as SHANDONG ZHONGXING MUSHROOM TECHNOLOGY CO., LTD
As of October 27, 2026, Shandong Zhongxing Mushroom Technology Co., Ltd (Dezhou, China) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for enoki mushroom, published by FDA on October 16, 2024, is also listed on Import Alert 99-35 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-23 · red listIA 99-35 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Shandong Zhongxing Mushroom Technology Co., Ltd
2 records, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 99-23red listEnoki MushroomSource
- Import alert listingListed on Import Alert 99-35red listEnoki MushroomsSource
Questions about Shandong Zhongxing Mushroom Technology Co., Ltd
- Is Shandong Zhongxing Mushroom Technology Co., Ltd on an FDA import alert?
- Yes. As of October 27, 2026, Shandong Zhongxing Mushroom Technology Co., Ltd is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for enoki mushroom; FDA published the listing on October 16, 2024.
- Has FDA refused shipments from Shandong Zhongxing Mushroom Technology Co., Ltd?
- No FDA import refusals for Shandong Zhongxing Mushroom Technology Co., Ltd appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Shandong Zhongxing Mushroom Technology Co., Ltd's FEI number?
- Shandong Zhongxing Mushroom Technology Co., Ltd's FDA Establishment Identifier (FEI) is 3026439459.
- Can shipments from Shandong Zhongxing Mushroom Technology Co., Ltd still enter the U.S.?
- Shipments of enoki mushroom from Shandong Zhongxing Mushroom Technology 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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