CLASS II Food recall · Reported 20 Aug 2025 · FDA Enforcement Report

PAX Spices & Labs products recalled

PAX Spices & Labs is recalling Product is. The recall was initiated on 1 Aug 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot#: 7I08242057; MFG Lot #: IO820WOG2057
Quantity recalled11,100 pounds

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0457-2025
FDA event ID
97384
Recalling firm
PAX Spices & Labs, Covina, CA
Brand
Product
Classification
Class II
Status
Terminated
Recall initiated
1 Aug 2025
FDA classified
12 Aug 2025
Reported
20 Aug 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Foreign Material
Product category
Other

Timeline

1 Aug 2025Recall initiated by company
12 Aug 2025Classified by FDA+11 days
20 Aug 2025Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Foreign object (metal) in granulated onion ingredient.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Product is distributed in bulk brown paper bags.

Where it was distributed

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

Questions about this recall

Why was it recalled?

Foreign object (metal) in granulated onion ingredient.

Which lots are affected?

Lot#: 7I08242057; MFG Lot #: IO820WOG2057

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other Other recalls

All 4,675