Class IITerminatedVoluntary: Firm initiated
Summit Import Corporation: food recall H-0671-2026
Summit Import Corporation of Jersey City, NJ recalled Spice Powder, 4 oz, Plastic Bag. Reason: Lead level was higher than NYSAGM Standard. The FDA listed it as Class II in its Enforcement Report dated Apr 29, 2026; distribution: Florida, Massachusetts, Maine, New Jersey, New York, Pennsylvania, South Carolina, Virginia.
Record status as published: Terminated (terminated Apr 23, 2026). 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
- Spice Powder, 4 oz, Plastic Bag
- Product quantity
- 20 cases
- Reason for recall
- Lead level was higher than NYSAGM Standard.
- Codes, lots and dates on the package
- 06204
- Distribution pattern
- The recalled product was distributed to the following states: NY, NJ, SC, ME, FL, PA, MA, VA
- 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
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Oct 17, 2024 |
| Classified by the FDA | Apr 23, 2026 |
| Published in the Enforcement Report | Apr 29, 2026 |
| Terminated | Apr 23, 2026 |
Other recalls by Summit Import Corporation
- F-0397-2025 · Jan 22, 2025 · Class II — Product tested and found high levels of lead.
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0671-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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