CLASS I Food recall · Reported 3 Sep 2014 · FDA Enforcement Report

Ground Oregano recalled by McCormick & Company

McCormick is recalling Ground Oregano, distributed in 39 states. The recall was initiated on 13 Aug 2014 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAUG 21 16H and AUG 22 16 H
Quantity recalled1032 cases

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-2397-2014
FDA event ID
69044
Recalling firm
McCormick, Hunt Valley, MD
Classification
Class I
Status
Terminated
Recall initiated
13 Aug 2014
FDA classified
27 Aug 2014
Reported
3 Sep 2014
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Salmonella
Product category
Spices

Timeline

13 Aug 2014Recall initiated by company
27 Aug 2014Classified by FDA+14 days
3 Sep 2014Published in enforcement report+7 days

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

Reason for recall

Retail sample of ground oregano tested positive for Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

McCormick Ground Oregano in 0.75 oz plastic bottle. UPC NUMBER: 52100003566 (as seen on label: 0-523561-6) MCCORMICK ITEM NUMBER: 900356

Where it was distributed

AL, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NH, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV

AlabamaArizonaCaliforniaColoradoFloridaGeorgiaHawaiiIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMarylandMichiganMinnesotaMissouriMississippi

Questions about this recall

Why was it recalled?

Retail sample of ground oregano tested positive for Salmonella.

Which lots are affected?

AUG 21 16H and AUG 22 16 H

Where was it sold?

AL, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NH, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV

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.

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