RecallHawk
Class I Recall

Nourish Inc. brand Fruit Snack Pack SNACK ATTACK 6.48 oz. Apples, Medjool Dates, Blackberries, Sunflower Butter Keep ref

Sodexo, DBA Nourish

Summary

The FDA issued a Class I for Nourish Inc. brand Fruit Snack Pack SNACK ATTACK 6.48 oz. Apples, Medjool Dates, by Sodexo, DBA Nourish. Reason: Undeclared peanut allergen.

Details

Source

Food Recall

External ID

F-0177-2023

Action Date

2022-11-30

Status

Terminated

Category

food

Product Description

Nourish Inc. brand Fruit Snack Pack SNACK ATTACK 6.48 oz. Apples, Medjool Dates, Blackberries, Sunflower Butter Keep refrigerated

Lot/Code Info: Expiration Date: 10/19/2022 - 10-21-2022

Quantity Affected: 188 units

Reason for Recall

Undeclared peanut allergen

Distribution

Product was distributed to 4 customers, all in CA.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-10-20

Company

Sodexo, DBA Nourish

Santa Clara, CA

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 28 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 (Sodexo, DBA Nourish) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Sodexo, DBA Nourish have FDA actions?

This is the only FDA action we have on record for Sodexo, DBA Nourish in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0177-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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