CLASS I Food recall · Reported 10 Jun 2020 · FDA Enforcement Report

Organic Ground Oregano recalled by K F K Seasonings

K F K Seasonings is recalling Organic Ground Oregano, distributed in Oregon, Utah. The recall was initiated on 8 May 2020 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLabel Lot # 121719 (for 50 lbs. case). Label Lot # 010920 (for 50 lbs. case). Label Lot # 020420 (for 40 lbs. case). The KFK's 6-digit lot coding is generally the date the order was submitted and input into KFK's system and may not align with actual production date.
Quantity recalled500 lbs.

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
F-0974-2020
FDA event ID
85640
Recalling firm
K F K Seasonings, Portland, OR
Classification
Class I
Status
Terminated
Recall initiated
8 May 2020
FDA classified
1 Jun 2020
Reported
10 Jun 2020
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Tree Nuts
Product category
Spices

Timeline

8 May 2020Recall initiated by company
1 Jun 2020Classified by FDA+24 days
10 Jun 2020Published in enforcement report+9 days

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

Reason for recall

Undeclared tree nuts and Crustacea.

Product as listed by the FDA

Organic Ground Oregano, Item # 90206. Packaged in 40 lbs. or 50 lbs. cases and sold under brand KFK Seasoning. This product contains Organic Oregano.

Where it was distributed

Distributed in OR and UT.

OregonUtah

Questions about this recall

Why was it recalled?

Undeclared tree nuts and Crustacea.

Which lots are affected?

Label Lot # 121719 (for 50 lbs. case). Label Lot # 010920 (for 50 lbs. case). Label Lot # 020420 (for 40 lbs. case). The KFK's 6-digit lot coding is generally the date the order was submitted and input into KFK's system and may not align with actual production date.

Where was it sold?

Distributed in OR and UT.

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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 products in this recall event

2 other products · FDA event 85640

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