Food Recall Check
Class I · High risk Terminated Initiated Jun 24, 2022 (4 years ago)

Organic Oregano Ground is packed in bulk recall

Recalled by OS Holding Inc · Portland, OR, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Ground organic oregano is recalled due to presence of Salmonella leeuwarden.

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Organic Oregano Ground is packed in bulk 35 lbs. cases with food-grade poly bag that is labeled in parts: "OREGONSPICE COMPANY***OG Oregano Ground***Net Wt 35 lb (15.89 kg)***13320 NE Jarrett St.*Portland, Oregon 97230***".

Quantity: 1,085 lbs.

Food: Spices & seasonings

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Oregon Spice Company (OSC) Output Lots: H008930 (Best By: 5/18/2023); H009569 (Best By: 5/27/2023); and H009908 (Best By: 6/2/2023).

Where it was sold

Arizona Minnesota Wisconsin

FDA's distribution note: Distributed in AZ, MN, and WI.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
OS Holding Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 24, 2022
In FDA report of
Jul 13, 2022
Terminated
Jul 27, 2022
FDA recall number
F-1388-2022 · event 90510
Official record
FDA enforcement report search

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