Food recall
Good Way Trading Group Inc recall: BaiLiFeng Dried Cinnamon Powder
Good Way Trading Group Inc, of Maspeth, NY, recalled BaiLiFeng Dried Cinnamon Powder. The FDA's reason: “contains high levels of lead (10.7 mg/kg).” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on October 24, 2025, and the FDA first listed it in its Enforcement Report of December 24, 2025. The recall is still going on.
How serious
Class II
It could cause temporary or minor harm
Why
Lead or other chemicals
Status
Ongoing
The recall
- Company
- Good Way Trading Group Inc (Maspeth, NY)
- Reason, in FDA's words
- “contains high levels of lead (10.7 mg/kg)”
- Where it was sold
- MA
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 97865
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
H-0313-2026 Class II
BaiLiFeng Dried Cinnamon Powder; Net Wt 4 oz/114G; Good Way Trading Group Inc 58-51 Maspeth Avenue Maspeth NY 11378; Product of China; Ingredients: Dried Cinnamon; UPC code: 4 897055 79940 1
Codes: Best by date: EXP.11.12.2026 ; Item 37514
Quantity: 150 bags
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Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of December 24, 2025.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.