RecallRadar
High RiskReported May 27, 2026 (5 weeks ago)

Squirrel Brand Travelers Mix 16 oz can UPC 07223899166

Recalled by JOHN B SANFILIPPO & SONS INC

Food recall

JOHN B SANFILIPPO & SONS INC

Class I — most serious

There is a reasonable chance that using this product could cause serious health problems or death.

See all recalls involving Salmonella

JOHN B SANFILIPPO & SONS INC has recalled Squirrel Brand Travelers Mix 16 oz can UPC 07223899166, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on May 27, 2026 and was initiated on May 5, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Squirrel Brand Travelers Mix 16 oz can UPC 07223899166, with approximately 3,858 cases affected. The company behind the recall is JOHN B SANFILIPPO & SONS INC, based in Elgin, IL. The FDA describes the product as: “Squirrel Brand Travelers Mix 16 oz can UPC 07223899166, 12 cans per case”

Why was Squirrel Brand Travelers Mix 16 oz can UPC 07223899166 recalled?

According to the FDA, the stated reason for the recall is: “potential presence of Salmonella.” In plain terms, this recall relates to Salmonella.

Salmonella is a group of bacteria that is one of the most common causes of foodborne illness in the United States. Public health authorities note that infections can lead to symptoms such as fever, diarrhea, and stomach cramps, and that young children, older adults, and people with weakened immune systems are at higher risk of serious illness. Because it can spread through contaminated food, regulators treat Salmonella findings seriously.

What should you do?

If you think you may have bought Squirrel Brand Travelers Mix 16 oz can UPC 07223899166, compare it against the product description and identifying codes (BEST BY 04/30/27 BEST BY 05/28/27 BEST BY 06/24/27) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact JOHN B SANFILIPPO & SONS INC or your local health authority.

About this recall

This recall was distributed in IL. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Ongoing
Date reported
May 27, 2026
Recall started
May 5, 2026
Distributed in
IL
What was recalled
Squirrel Brand Travelers Mix 16 oz can UPC 07223899166, 12 cans per case
Why it was recalled (as stated by the FDA)
potential presence of Salmonella
How to identify the affected product
BEST BY 04/30/27 BEST BY 05/28/27 BEST BY 06/24/27
Amount recalled
3,858 cases

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Squirrel Brand Travelers Mix 16 oz can UPC 07223899166 recalled?+

According to the FDA: potential presence of Salmonella

How serious is this recall?+

Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.

What should I do if I have Squirrel Brand Travelers Mix 16 oz can UPC 07223899166?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0833-2026. Information last synced from the FDA on July 6, 2026.

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