RecallHawk
Class I Recall

Sun Sprouts Alfalfa Sprouts packaged in 4 oz plastic clamshell, 6/4 oz or 12/4 oz containers per case; Sun Sprouts Alfal

Rhodes Legacy, Inc.

Summary

The FDA issued a Class I for Sun Sprouts Alfalfa Sprouts packaged in 4 oz plastic clamshell, 6/4 oz or 12/4 o by Rhodes Legacy, Inc.. Reason: Alfalfa sprouts have the potential to be contaminated with Salmonella..

Details

Source

Food Recall

External ID

F-0290-2023

Action Date

2023-01-25

Status

Terminated

Category

food

Product Description

Sun Sprouts Alfalfa Sprouts packaged in 4 oz plastic clamshell, 6/4 oz or 12/4 oz containers per case; Sun Sprouts Alfalfa Sprouts packaged in 2.5lb plastic lined box.

Lot/Code Info: Lot 4211, Sell by date 12/10/22 through 12/14/22; Lot 5211, Sell by date 12/17/22 through 12/27/22; Lot 3212, Sell by date 12/26/22 through 12/31/22; Lot 4212; Sell by date 1/3/23 through 1/7/23.

Quantity Affected: 1406 lbs

Reason for Recall

Alfalfa sprouts have the potential to be contaminated with Salmonella.

Distribution

Sold to distributors and a retailer in Nebraska, Kansas, and Iowa.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-12-28

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 84 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 (Rhodes Legacy, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Rhodes Legacy, Inc. have FDA actions?

This is the only FDA action we have on record for Rhodes Legacy, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0290-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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