RecallHawk
Class II Recall

GOLD GARLIC POWDER IRRADIATED; NET WT. 50 LBS; PRODUCT OF CHINA

Pacific Meridian Group, LLC

Summary

The FDA issued a Class II for GOLD GARLIC POWDER IRRADIATED; NET WT. 50 LBS; PRODUCT OF CHINA by Pacific Meridian Group, LLC. Reason: Potential contamination with foreign objects (metal).

Details

Source

Food Recall

External ID

F-0731-2025

Action Date

2025-04-30

Status

Ongoing

Category

food

Product Description

GOLD GARLIC POWDER IRRADIATED; NET WT. 50 LBS; PRODUCT OF CHINA

Lot/Code Info: Lot, Expiration: LN11842024211IR, 7/29/2026; LN11842024212IR, 7/30/2026; LN11842024248IR, 9/4/2026; LN11842024249IR, 9/5/2026

Quantity Affected: 175,000 lbs

Reason for Recall

Potential contamination with foreign objects (metal)

Distribution

CA, IL, TX

Type: Voluntary: Firm initiated

Recall Initiated: 2025-03-17

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 35 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Pacific Meridian Group, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Pacific Meridian Group, LLC have FDA actions?

This is the only FDA action we have on record for Pacific Meridian Group, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0731-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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