RecallHawk
Class I Recall

Great Value Honey Roasted Cashews, 8.25oz. plastic can, UPC 0 78742 13334 8

John B. Sanfilippo & Son Inc.

Summary

The FDA issued a Class I for Great Value Honey Roasted Cashews, 8.25oz. plastic can, UPC 0 78742 13334 8 by John B. Sanfilippo & Son Inc.. Reason: undeclared milk and coconut.

Details

Source

Food Recall

External ID

F-1099-2024

Action Date

2024-04-03

Status

Terminated

Category

food

Product Description

Great Value Honey Roasted Cashews, 8.25oz. plastic can, UPC 0 78742 13334 8

Lot/Code Info: Best if Used By: JUL 08, 2025

Quantity Affected: 17,184 cans

Reason for Recall

undeclared milk and coconut

Distribution

AL, AR, CA, CO, CT, FL, GA, HI, IL, IN, KS, KY, LA, MA, MO, MS, NC, NE, NJ, NM, NV, NY, OH, OK, PA, SC, TN, TX, VT, WV

Type: Voluntary: Firm initiated

Recall Initiated: 2024-03-07

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 40 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 & Son 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 & Son Inc. have FDA actions?

This is the only FDA action we have on record for John B. Sanfilippo & Son Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1099-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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