BaiLiFeng Dried Cinnamon Powder; Net Wt 4 oz/114G; Good Way Trading Group Inc 58-51 Maspeth Avenue Maspeth NY 11378; Pro
Summary
The FDA issued a Class II for BaiLiFeng Dried Cinnamon Powder; Net Wt 4 oz/114G; Good Way Trading Group Inc 58 by Good Way Trading Group Inc. Reason: contains high levels of lead (10.7 mg/kg).
Details
Source
Food Recall
External ID
H-0313-2026
Action Date
2025-12-24
Status
Ongoing
Category
food
Product Description
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
Lot/Code Info: Best by date: EXP.11.12.2026 ; Item 37514
Quantity Affected: 150 bags
Reason for Recall
contains high levels of lead (10.7 mg/kg)
Distribution
MA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-24
Company
Maspeth, NY
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 87 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Good Way Trading Group Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Good Way Trading Group Inc have FDA actions?
This is the only FDA action we have on record for Good Way Trading Group Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0313-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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