RecallHawk
Class II Recall

Butter Flavored Popcorn Naturally & Artificially Flavored, 8oz. UPC: 70175 06021 Packaged in clear plastic bags, 9 bags

Bickel's Snack Foods Inc

Summary

The FDA issued a Class II for Butter Flavored Popcorn Naturally & Artificially Flavored, 8oz. UPC: 70175 06021 by Bickel's Snack Foods Inc. Reason: Undeclared milk.

Details

Source

Food Recall

External ID

F-1457-2023

Action Date

2023-08-30

Status

Terminated

Category

food

Product Description

Butter Flavored Popcorn Naturally & Artificially Flavored, 8oz. UPC: 70175 06021 Packaged in clear plastic bags, 9 bags per case.

Lot/Code Info: 20 NOV 23 Z4 E1 and 27 NOV 23 Z4 E1

Quantity Affected: 6,048 bags

Reason for Recall

Undeclared milk

Distribution

Distributed in GA and retails stores nationwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-08-08

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 63 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Bickel's Snack 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 Bickel's Snack Foods Inc have FDA actions?

This is the only FDA action we have on record for Bickel's Snack Foods Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1457-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions