RecallHawk
Class I Recall

Everything Sprouts Robust Radish Mix, Net Wt. 5.0 oz (142 g) UPC 0 87906-00007 5. Keep Refrigerated. everythingsprouts

Everything Sprouts, LLC

Summary

The FDA issued a Class I for Everything Sprouts Robust Radish Mix, Net Wt. 5.0 oz (142 g) UPC 0 87906-00007 5 by Everything Sprouts, LLC. Reason: Sprouts may be contaminated with STEC E. coli and/or Salmonella..

Details

Source

Food Recall

External ID

H-1340-2026

Action Date

2026-09-23

Status

Ongoing

Category

food

Product Description

Everything Sprouts Robust Radish Mix, Net Wt. 5.0 oz (142 g) UPC 0 87906-00007 5. Keep Refrigerated. everythingsprouts.com

Lot/Code Info: Lot# 223, 226, 230, 233

Quantity Affected: 278.44 lbs.

Reason for Recall

Sprouts may be contaminated with STEC E. coli and/or Salmonella.

Distribution

MN, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2026-08-22

Company

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 54 food recalls issued in the same week, part of 82 food-related FDA actions this month.

Everything Sprouts, LLC has 4 FDA actions in our database, including 4 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 (Everything Sprouts, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Everything Sprouts, LLC have FDA actions?

Everything Sprouts, LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1340-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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