RecallHawk
Class I Recall

GE 24777800000 Brownie Classic Peanut Bttr 8c , 14Oz

Giant Eagle

Summary

The FDA issued a Class I for GE 24777800000 Brownie Classic Peanut Bttr 8c , 14Oz by Giant Eagle. Reason: Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination..

Details

Source

Food Recall

External ID

F-1394-2022

Action Date

2022-07-13

Status

Terminated

Category

food

Product Description

GE 24777800000 Brownie Classic Peanut Bttr 8c , 14Oz

Lot/Code Info: GE 24777800000 Brownie Classic Peanut Bttr 8c 14Oz

Quantity Affected: 15 Units

Reason for Recall

Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.

Distribution

The product was distributed domestically to the following State: PA

Type: Voluntary: Firm initiated

Recall Initiated: 2022-05-23

Company

Giant Eagle

Pittsburgh, PA

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

Giant Eagle has 11 FDA actions in our database, including 11 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 (Giant Eagle) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Giant Eagle have FDA actions?

Giant Eagle has 11 FDA actions in our database, including 11 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1394-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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