RecallHawk
Class I Recall

Pure Ground Ingredients Organic Oregano Leaf Powder Item#: OREO-PW Weight: 35 LBS/15.89 kgs Processed and Packaged at Pu

Pure Ground Ingredients

Summary

The FDA issued a Class I for Pure Ground Ingredients Organic Oregano Leaf Powder Item#: OREO-PW Weight: 35 LB by Pure Ground Ingredients. Reason: Potential Salmonella contamination..

Details

Source

Food Recall

External ID

F-1403-2022

Action Date

2022-07-13

Status

Terminated

Category

food

Product Description

Pure Ground Ingredients Organic Oregano Leaf Powder Item#: OREO-PW Weight: 35 LBS/15.89 kgs Processed and Packaged at Pure Ground Ingredients 2535 Business Parkway Minden, NV 89423 Certified Organics By CCOF Organic Oregano Leaf Ground Item#: OREO-GR Weight: 35 LBS/15.89 kgs Processed and Packaged at Pure Ground Ingredients 2535 Business Parkway Minden, NV 89423 Certified Organics By CCOF

Lot/Code Info: Organic Oregano Leaf Powder Lot Number: OREO-1302392MR-PW-938J , OREO-1302392PW-938J Expiration Date: April 2024 Organic Oregano Leaf Ground Lot Number: OREO-1302392MR-GR-938J Expiration Date: April 2024

Quantity Affected: 4,833 lbs.

Reason for Recall

Potential Salmonella contamination.

Distribution

U.S. distribution to the following: OR, WI, MD, CO. No foreign distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-06-23

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 53 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Pure Ground Ingredients) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Pure Ground Ingredients have FDA actions?

This is the only FDA action we have on record for Pure Ground Ingredients in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1403-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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