CLASS II ONGOING Food recall · Reported 24 Dec 2025 · FDA Enforcement Report
BaiLiFeng Dried Cinnamon Powder recalled by Good Way Trading Group
Good Way Trading Group is recalling BaiLiFeng Dried Cinnamon Powder, distributed in Massachusetts. The recall was initiated on 24 Oct 2025 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0313-2026
- FDA event ID
- 97865
- Recalling firm
- Good Way Trading Group, Maspeth, NY
- Brand
- BaiLiFeng
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 24 Oct 2025
- FDA classified
- 17 Dec 2025
- Reported
- 24 Dec 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Lead & Heavy Metals
- Product category
- Fish
Timeline
| 24 Oct 2025 | Recall initiated by company | |
| 17 Dec 2025 | Classified by FDA | +54 days |
| 24 Dec 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
contains high levels of lead (10.7 mg/kg)
Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.
Product as listed by the FDA
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
Where it was distributed
MA
Questions about this recall
Why was it recalled?
contains high levels of lead (10.7 mg/kg)
Which lots are affected?
Best by date: EXP.11.12.2026 ; Item 37514
Where was it sold?
MA
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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