Class IITerminatedVoluntary: Firm initiated
Summit Import Corporation: food recall F-0397-2025
Summit Import Corporation of Jersey City, NJ recalled Yu Yee, Five Spice Powder,1.76oz. Reason: Product tested and found high levels of lead. The FDA listed it as Class II in its Enforcement Report dated Jan 22, 2025; distribution: Alaska, Connecticut, Florida, Georgia, Iowa, Massachusetts, Maryland, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, South Carolina, Virginia.
Record status as published: Terminated (terminated Feb 19, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Yu Yee, Five Spice Powder,1.76oz
- Product quantity
- 62 cases
- Reason for recall
- Product tested and found high levels of lead.
- Codes, lots and dates on the package
- 06072/WH538
- Distribution pattern
- The product was distributed to the following states: NY, VA, CT, FL, OH, SC, AK, MA, NJ, GA, MN, MO, IA, PA, MD, Bahamas
- Recalling firm
- Summit Import Corporation, Jersey City, NJ
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Telephone
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 10, 2024 |
| Classified by the FDA | Jan 14, 2025 |
| Published in the Enforcement Report | Jan 22, 2025 |
| Terminated | Feb 19, 2025 |
Other recalls by Summit Import Corporation
- H-0671-2026 · Apr 29, 2026 · Class II — Lead level was higher than NYSAGM Standard.
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0397-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.