RecallHawk
Class II Recall

Giant Eagle, Diced Green Peppers, 10 oz. poly bags and 22# cases, also poly bags and cartons, 12/10 oz. bags per case an

Frozen Food Development

Summary

The FDA issued a Class II for Giant Eagle, Diced Green Peppers, 10 oz. poly bags and 22# cases, also poly bags by Frozen Food Development. Reason: Frozen Food Development, Lancaster, PA is initiating a recall of Giant Eagle, Diced Green Peppers, 10 oz. poly bags and 22# cases (12/10 oz. bags per .

Details

Source

Food Recall

External ID

F-0356-2022

Action Date

2022-01-05

Status

Terminated

Category

food

Product Description

Giant Eagle, Diced Green Peppers, 10 oz. poly bags and 22# cases, also poly bags and cartons, 12/10 oz. bags per case and bulk 22 lbs. bags

Lot/Code Info: R16372 exp. 03/12/2023 R16514 exp. 09/30/2022 R17422 exp. 01/21/2023 R17117 exp.. 08/12/2023 R17133 exp. 04/14/2023 R18388 exp. 10/14/2023

Quantity Affected: 20,825 lbs.

Reason for Recall

Frozen Food Development, Lancaster, PA is initiating a recall of Giant Eagle, Diced Green Peppers, 10 oz. poly bags and 22# cases (12/10 oz. bags per case) and bulk 22 lbs. bags because they tested positive for Listeria Monocytogenes.

Distribution

The product was distributed to three direct Accounts in the United States.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-11-30

Company

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 54 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 (Frozen Food Development) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Frozen Food Development have FDA actions?

This is the only FDA action we have on record for Frozen Food Development in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0356-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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