CLASS I ONGOING Food recall · Reported 29 Aug 2018 · FDA Enforcement Report

Peanut Paste/Butter bulk tankers recalled by Peanut Processors

Peanut Processors is recalling Peanut Paste/Butter bulk tankers, distributed in Arkansas, Tennessee. The recall was initiated on 20 Jul 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot#: E-18191 & Lot#: E-18191-1
Quantity recalled93,620 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-1840-2018
FDA event ID
80599
Recalling firm
Peanut Processors, Dublin, NC
Classification
Class I
Status
Ongoing
Recall initiated
20 Jul 2018
FDA classified
21 Aug 2018
Reported
29 Aug 2018
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Salmonella
Product category
Butter

Timeline

20 Jul 2018Recall initiated by company
21 Aug 2018Classified by FDA+32 days
29 Aug 2018Published in enforcement report+8 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 a customer that the product test 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

Peanut Paste/Butter bulk tankers

Where it was distributed

Product was shipped to AR & TN.

ArkansasTennessee

Questions about this recall

Why was it recalled?

The firm was notified by a customer that the product test positive for Salmonella

Which lots are affected?

Lot#: E-18191 & Lot#: E-18191-1

Where was it sold?

Product was shipped to AR & TN.

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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