RecallHawk
Class III Recall

Simply Nature Organic Spring Mix 16 oz. Marketside Spring Mix 11 oz. and 5 oz.

Dole Fresh Vegetables Inc

Summary

The FDA issued a Class III for Simply Nature Organic Spring Mix 16 oz. Marketside Spring Mix 11 oz. and 5 oz. by Dole Fresh Vegetables Inc. Reason: Potential to contain hairy nightshade..

Details

Source

Food Recall

External ID

F-1512-2022

Action Date

2022-08-03

Status

Terminated

Category

food

Product Description

Simply Nature Organic Spring Mix 16 oz. Marketside Spring Mix 11 oz. and 5 oz.

Lot/Code Info: 11oz Marketside Spring Mix: W167011 with BIUB: 6/30/2022 5oz Marketside Spring Mix: W16709A and W16709B with BIUB: 6/29/2022 16 oz Simply Nature Organic Spring Mix: W167011 with BIUB: 6/30/2022 16 oz Simply Nature Organic Spring Mix: W168011 with BIUB: 7/01/2022

Quantity Affected: 1647 cases

Reason for Recall

Potential to contain hairy nightshade.

Distribution

U.S. distribution to the following: OH, IL, IN, TN No foreign distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-06-25

Company

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 84 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Dole Fresh Vegetables Inc has 160 FDA actions in our database, including 160 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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

How often does Dole Fresh Vegetables Inc have FDA actions?

Dole Fresh Vegetables Inc has 160 FDA actions in our database, including 160 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1512-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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