RecallHawk
Class II Recall

Birds Eye Broccoli Tots, frozen, 12OZ bag UPC 00-0-14500-00125-2

CONAGRA BRANDS

Summary

The FDA issued a Class II for Birds Eye Broccoli Tots, frozen, 12OZ bag UPC 00-0-14500-00125-2 by CONAGRA BRANDS. Reason: Small rocks and metal fragments in the product.

Details

Source

Food Recall

External ID

F-0270-2022

Action Date

2021-12-15

Status

Terminated

Category

food

Product Description

Birds Eye Broccoli Tots, frozen, 12OZ bag UPC 00-0-14500-00125-2

Lot/Code Info: Batch/Lot Code and Best By Date: 4715105620 AUG-19-2022 and AUG-25-2022 4715104220 AUG-11-2022 and AUG-12-2022 4715113720 NOV-17-2022 4715113020 NOV-10-2022

Quantity Affected: 185,750 Bags

Reason for Recall

Small rocks and metal fragments in the product

Distribution

nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2021-11-19

Company

CONAGRA BRANDS

Chicago, IL

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

CONAGRA BRANDS has 3 FDA actions in our database, including 3 recalls.

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

How often does CONAGRA BRANDS have FDA actions?

CONAGRA BRANDS has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0270-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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