CLASS I Food recall · Reported 31 Mar 2021 · FDA Enforcement Report

Nutrin/Amendobras Roasted Peanut Splits recalled by Nutrin Distribution

Nutrin Distribution is recalling Nutrin/Amendobras Roasted Peanut Splits, distributed in Pennsylvania. The recall was initiated on 27 Feb 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesTOR0043/20
Quantity recalled40,500 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-0348-2021
FDA event ID
87469
Recalling firm
Nutrin Distribution, Washington, DC
Brand
Nutrin
Classification
Class I
Status
Terminated
Recall initiated
27 Feb 2021
FDA classified
19 Mar 2021
Reported
31 Mar 2021
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Salmonella
Product category
Peanuts

Timeline

27 Feb 2021Recall initiated by company
19 Mar 2021Classified by FDA+20 days
31 Mar 2021Published in enforcement report+12 days

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

Reason for recall

Possible Salmonella contamination in roasted peanut splits

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

Nutrin/Amendobras brand Roasted Peanut Splits packaged in 30lb cardboard boxes.

Where it was distributed

Distributed to one customer in PA

Pennsylvania

Questions about this recall

Why was it recalled?

Possible Salmonella contamination in roasted peanut splits

Which lots are affected?

TOR0043/20

Where was it sold?

Distributed to one customer in PA

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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