Ningbo Songxin Foodstuffs Co., Ltd
FDA import alert and refusal historyNingbo, ChinaFEI 3010150476
Recorded by FDA as NINGBO SONGXIN FOODSTUFFS CO., LTD
As of October 27, 2026, Ningbo Songxin Foodstuffs Co., Ltd (Ningbo, China) is on the red list of FDA Import Alert 99-42 (Foods: heavy metal (toxic element) contamination) for canned mandarin orange in light syrup, published by FDA on March 17, 2026, and has 2 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
- Orange (citrus) · PB-FOOD
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ningbo Songxin Foodstuffs Co., Ltd
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
Questions about Ningbo Songxin Foodstuffs Co., Ltd
- Is Ningbo Songxin Foodstuffs Co., Ltd on an FDA import alert?
- Yes. As of October 27, 2026, Ningbo Songxin Foodstuffs Co., Ltd is on the red list of FDA Import Alert 99-42, “Foods: heavy metal (toxic element) contamination”, for canned mandarin orange in light syrup; FDA published the listing on March 17, 2026.
- Has FDA refused shipments from Ningbo Songxin Foodstuffs Co., Ltd?
- Yes. FDA refused 2 shipment lines from Ningbo Songxin Foodstuffs Co., Ltd between March 3, 2026 and September 14, 2026. The most recent, on September 14, 2026, was orange (citrus), charged as PB-FOOD (pb-food).
- Why did FDA refuse Ningbo Songxin Foodstuffs Co., Ltd's shipments?
- The most frequent charges are PB-FOOD (pb-food, 1 line) and POISONOUS (poisonous or deleterious substance, 1 line).
- What is Ningbo Songxin Foodstuffs Co., Ltd's FEI number?
- Ningbo Songxin Foodstuffs Co., Ltd's FDA Establishment Identifier (FEI) is 3010150476.
- Can shipments from Ningbo Songxin Foodstuffs Co., Ltd still enter the U.S.?
- Shipments of canned mandarin orange in light syrup from Ningbo Songxin Foodstuffs 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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