RecallHawk
Class I Recall

Pop a Nosh Mixed Munch; Honey BBQ Flavor; 8oz plastic bag; Potato Chips, Popcorn, Pretzels; UPC 914669941

AMB FOODS INC

Summary

The FDA issued a Class I for Pop a Nosh Mixed Munch; Honey BBQ Flavor; 8oz plastic bag; Potato Chips, Popcorn by AMB FOODS INC. Reason: Products contain undeclared wheat..

Details

Source

Food Recall

External ID

F-1425-2024

Action Date

2024-07-03

Status

Terminated

Category

food

Product Description

Pop a Nosh Mixed Munch; Honey BBQ Flavor; 8oz plastic bag; Potato Chips, Popcorn, Pretzels; UPC 914669941

Lot/Code Info: All product that does not include allergen information.

Quantity Affected: 2,100 units (total)

Reason for Recall

Products contain undeclared wheat.

Distribution

New York

Type: Voluntary: Firm initiated

Recall Initiated: 2024-05-24

Company

AMB FOODS INC

Brooklyn, NY

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

AMB FOODS INC has 2 FDA actions in our database, including 2 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 (AMB FOODS INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does AMB FOODS INC have FDA actions?

AMB FOODS INC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1425-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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