CLASS I Food recall · Reported 21 Dec 2016 · FDA Enforcement Report

Hickory Harvest Foods Rucker's Cajun Mix bag recalled

Ohio Hickory Harvest Brand Products is recalling Hickory Harvest Foods Rucker's Cajun Mix bag in a box Ingredients: Cajun Sesame, distributed in 43 states. The recall was initiated on 4 May 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest if Used By: 110415, 021116, 031016, 042315, 070115, 080415, 080615, 082715, 090315, 092415, 100615, 120315;
Quantity recalled685/25 lb. bags in boxes

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-0319-2017
FDA event ID
74039
Recalling firm
Ohio Hickory Harvest Brand Products, Akron, OH
Classification
Class I
Status
Terminated
Recall initiated
4 May 2016
FDA classified
10 Dec 2016
Reported
21 Dec 2016
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Peanuts

Timeline

4 May 2016Recall initiated by company
10 Dec 2016Classified by FDA+220 days
21 Dec 2016Published in enforcement report+11 days

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

Reason for recall

The firm was notified by their supplier that the products may be contaminated with Listeria monocytogenes..

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Hickory Harvest FOODS Rucker's Cajun Mix 25 lb. bag in a box INGREDIENTS: Cajun Sesame Sticks***soybean oil***Sunflower Kernels, Hot & Spicy Peanuts***Contains: Peanut, Soy, Wheat.

Where it was distributed

Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI & WY.

AlabamaArkansasArizonaCaliforniaColoradoConnecticutFloridaGeorgiaIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMarylandMaineMichiganMissouri

Questions about this recall

Why was it recalled?

The firm was notified by their supplier that the products may be contaminated with Listeria monocytogenes..

Which lots are affected?

Best if Used By: 110415, 021116, 031016, 042315, 070115, 080415, 080615, 082715, 090315, 092415, 100615, 120315;

Where was it sold?

Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI & WY.

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

5 other products · FDA event 74039

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