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Class II: temporary or reversible health riskTerminated

PAX Spices & Labs Product is distributed in bulk brown paper Recall

Product is distributed in bulk brown paper bags

PAX Spices & Labs Inc · Covina, CA

Risk level
Class II
Reported by FDA
Aug 20, 2025
Recall ID
H-0457-2025
Check your lot numberHow we source this data

Summary

PAX Spices & Labs recalled Product is distributed in bulk brown paper starting Aug 1, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report H-0457-2025 on Aug 20, 2025. Reason: Foreign object (metal) in granulated onion ingredient. Status: Terminated.

Why it was recalled

Foreign object (metal) in granulated onion ingredient.

Product description

Product is distributed in bulk brown paper bags.

Lot numbers, UPCs & expiration codes

Lot#: 7I08242057; MFG Lot #: IO820WOG2057

Where it was sold

Product is distributed to 10 customers who further process ingredient into a final product.

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-0457-2025
Classification
Class II
Status
Terminated
Recall initiated
Aug 1, 2025
FDA report date
Aug 20, 2025
Quantity
11,100 pounds
Recall type
Voluntary: Firm initiated
Recalling firm
PAX Spices & Labs Inc

Original FDA data

Every field from FDA enforcement report H-0457-2025, exactly as published.

Show all FDA fields
City
Covina
State
CA
Status
Terminated
Country
United States
Event ID
97384
Address
550 N Rimsdale Ave
Code information
Lot#: 7I08242057; MFG Lot #: IO820WOG2057
Postal code
91722-3507
Report date
Aug 20, 2025
Product type
Food
Recall number
H-0457-2025
Classification
Class II
Recalling firm
PAX Spices & Labs Inc
Product quantity
11,100 pounds
Termination date
Sep 18, 2025
Reason for recall
Foreign object (metal) in granulated onion ingredient.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Product is distributed in bulk brown paper bags.
Distribution pattern
Product is distributed to 10 customers who further process ingredient into a final product.
Recall initiation date
Aug 1, 2025
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Aug 12, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0457-2025, published Aug 20, 2025. View the source record (openFDA) · FDA enforcement reports

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

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