CLASS I ONGOING Food recall · Reported 27 May 2026 · FDA Enforcement Report

Good & Gather Mexican Street Corn Trail Mix recalled

John B Sanfilippo & Sons is recalling Good & Gather Mexican Street Corn Trail Mix, distributed nationwide in the US. The recall was initiated on 5 May 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBEST BY 23/MAR/2027 GY
Quantity recalled272 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
H-0835-2026
FDA event ID
98919
Recalling firm
John B Sanfilippo & Sons, Elgin, IL
Brand
Good
Classification
Class I
Status
Ongoing
Recall initiated
5 May 2026
FDA classified
21 May 2026
Reported
27 May 2026
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
Nuts

Timeline

5 May 2026Recall initiated by company
21 May 2026Classified by FDA+16 days
27 May 2026Published in enforcement report+6 days

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

Reason for recall

potential presence of 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

Good & Gather Mexican Street Corn Trail Mix 8 oz bag UPC 085239270240, 8 bags per case

Where it was distributed

Nationwide

Nationwide

Stores named: Target

Questions about this recall

Why was it recalled?

potential presence of Salmonella

Which lots are affected?

BEST BY 23/MAR/2027 GY

Where was it sold?

Nationwide

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 98919

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