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Class II: temporary or reversible health riskTerminated

Summit Import Spice Powder Recall

Spice Powder, 4 oz, Plastic Bag

Summit Import Corporation · Jersey City, NJ

Risk level
Class II
Reported by FDA
Apr 29, 2026
Recall ID
H-0671-2026
Check your lot numberHow we source this data

Summary

Summit Import recalled Spice Powder starting Oct 17, 2024. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report H-0671-2026 on Apr 29, 2026. Reason: Lead level was higher than NYSAGM Standard. Status: Terminated.

Why it was recalled

Lead level was higher than NYSAGM Standard.

Product description

Spice Powder, 4 oz, Plastic Bag

Lot numbers, UPCs & expiration codes

06204

Where it was sold

The recalled product was distributed to the following states: NY, NJ, SC, ME, FL, PA, MA, VA

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-0671-2026
Classification
Class II
Status
Terminated
Recall initiated
Oct 17, 2024
FDA report date
Apr 29, 2026
Quantity
20 cases
Recall type
Voluntary: Firm initiated
Recalling firm
Summit Import Corporation

Original FDA data

Every field from FDA enforcement report H-0671-2026, exactly as published.

Show all FDA fields
City
Jersey City
State
NJ
Status
Terminated
Country
United States
Event ID
97213
Address
100 Summit Pl
Code information
06204
Postal code
07305-4524
Report date
Apr 29, 2026
Product type
Food
Recall number
H-0671-2026
Classification
Class II
Recalling firm
Summit Import Corporation
Product quantity
20 cases
Termination date
Apr 23, 2026
Reason for recall
Lead level was higher than NYSAGM Standard.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Spice Powder, 4 oz, Plastic Bag
Distribution pattern
The recalled product was distributed to the following states: NY, NJ, SC, ME, FL, PA, MA, VA
Recall initiation date
Oct 17, 2024
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Apr 23, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0671-2026, published Apr 29, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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