Zhongshan Mcpl Zhengfeng Dried Fruit Foodstuffs I/e Co., Ltd
FDA import alert and refusal historyZhongshan, ChinaFEI 3004298792
As of October 26, 2026, Zhongshan Mcpl Zhengfeng Dried Fruit Foodstuffs I/e Co., Ltd (Zhongshan, China) is on the red list of FDA Import Alert 99-42 (Foods: heavy metal (toxic element) contamination) for plums, published by FDA on October 13, 2022, 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 99-42 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Zhongshan Mcpl Zhengfeng Dried Fruit Foodstuffs I/e Co., Ltd
1 record, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 99-42red listPlumsSource
Questions about Zhongshan Mcpl Zhengfeng Dried Fruit Foodstuffs I/e Co., Ltd
- Is Zhongshan Mcpl Zhengfeng Dried Fruit Foodstuffs I/e Co., Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Zhongshan Mcpl Zhengfeng Dried Fruit Foodstuffs I/e Co., Ltd is on the red list of FDA Import Alert 99-42, “Foods: heavy metal (toxic element) contamination”, for plums; FDA published the listing on October 13, 2022.
- Has FDA refused shipments from Zhongshan Mcpl Zhengfeng Dried Fruit Foodstuffs I/e Co., Ltd?
- No FDA import refusals for Zhongshan Mcpl Zhengfeng Dried Fruit Foodstuffs I/e Co., Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Zhongshan Mcpl Zhengfeng Dried Fruit Foodstuffs I/e Co., Ltd's FEI number?
- Zhongshan Mcpl Zhengfeng Dried Fruit Foodstuffs I/e Co., Ltd's FDA Establishment Identifier (FEI) is 3004298792.
- Can shipments from Zhongshan Mcpl Zhengfeng Dried Fruit Foodstuffs I/e Co., Ltd still enter the U.S.?
- Shipments of plums from Zhongshan Mcpl Zhengfeng Dried Fruit Foodstuffs I/e Co., Ltd can be detained without physical examination under Import Alert 99-42; 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.