RecallHawk
Class I Recall

Nature's Heart Mango Turmeric Cashew Glazed Mix 1.5oz poly film pouches - 32 units per case

Nestle Usa Inc

Summary

The FDA issued a Class I for Nature's Heart Mango Turmeric Cashew Glazed Mix 1.5oz poly film pouches - 32 un by Nestle Usa Inc. Reason: Undeclared Allergen - Peanuts.

Details

Source

Food Recall

External ID

F-0074-2022

Action Date

2021-11-03

Status

Terminated

Category

food

Product Description

Nature's Heart Mango Turmeric Cashew Glazed Mix 1.5oz poly film pouches - 32 units per case

Lot/Code Info: Batch Codes: 1089T353T2, 1090T353T2, 1091T353T2 Product Numbers: 12456681 Manufacturer Number: 10011496344 Best By Date: DEC 2021, JAN 2022, FEB 2022, & APR 2022

Quantity Affected: 1102 cases

Reason for Recall

Undeclared Allergen - Peanuts

Distribution

AL,AR,CA,CO,CT,FL,GA,IA,IL,IN,KY,LA,MA,MD,MI,MN,MS,NC,NE,NH,NJ,NV,NY,OH,OR,PA, SC,TN,TX,UT,VA,WA

Type: Voluntary: Firm initiated

Recall Initiated: 2021-10-07

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

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

How often does Nestle Usa Inc have FDA actions?

Nestle Usa Inc 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 "F-0074-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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