Class IITerminatedVoluntary: Firm initiated
PAX Spices & Labs Inc: food recall H-0457-2025
PAX Spices & Labs Inc of Covina, CA recalled Product is distributed in bulk brown paper bags. Reason: Foreign object (metal) in granulated onion ingredient. The FDA listed it as Class II in its Enforcement Report dated Aug 20, 2025.
Record status as published: Terminated (terminated Sep 18, 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
- Product is distributed in bulk brown paper bags.
- Product quantity
- 11,100 pounds
- Reason for recall
- Foreign object (metal) in granulated onion ingredient.
- Codes, lots and dates on the package
- Lot#: 7I08242057; MFG Lot #: IO820WOG2057
- Distribution pattern
- Product is distributed to 10 customers who further process ingredient into a final product.
- Recalling firm
- PAX Spices & Labs Inc, Covina, CA
- 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 | Aug 1, 2025 |
| Classified by the FDA | Aug 12, 2025 |
| Published in the Enforcement Report | Aug 20, 2025 |
| Terminated | Sep 18, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0457-2025 (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.