Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar UPC 085839073319 and 36 oz plastic jar UPC 085839071483. 23 oz
Summary
The FDA issued a Class I for Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar UPC 085839073319 and 36 by JOHN B SANFILIPPO & SONS INC. Reason: potential presence of Salmonella.
Details
Source
Food Recall
External ID
H-0831-2026
Action Date
2026-05-27
Status
Ongoing
Category
food
Product Description
Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar UPC 085839073319 and 36 oz plastic jar UPC 085839071483. 23 oz 6 jars per case case and 96 jars per display. 36 oz 6 jars per case
Lot/Code Info: BEST BY 01/28/27 BEST BY 02/05/27 BEST BY 02/12/27 BEST BY 02/17/27 BEST BY 03/03/27 BEST BY 03/14/27 BEST BY 02/05/27 BEST BY 26/FEB/2027 BEST BY 13/MAR/2027 BEST BY 02/APR/2027
Quantity Affected: 33,176 cases and 22 displays
Reason for Recall
potential presence of Salmonella
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-05
Company
Elgin, IL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 80 food recalls issued in the same week, part of 204 food-related FDA actions this month.
JOHN B SANFILIPPO & SONS INC has 6 FDA actions in our database, including 6 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (JOHN B SANFILIPPO & SONS INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does JOHN B SANFILIPPO & SONS INC have FDA actions?
JOHN B SANFILIPPO & SONS INC has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0831-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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