Giant Eagle Recall: Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination. - F-1395-2022

🇺🇸 United States

1. May 23, 2022 - Recall initiated
2. July 13, 2022 - Reported by source
3. November 3, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1395-2022

Event ID

90334

Status

Terminated

Classification

Class I

Company

Giant Eagle

Product description

GE 25022900000 Peanut Butter Fudge Bar Cake 22.6 Oz

Quantity

12 Units

Reason

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

Recall initiation date

May 23, 2022

Report date

July 13, 2022

Classification date

Not published in this source record

Termination date

November 3, 2022

Distribution pattern

The product was distributed domestically to the following State: PA

UPC, lot, and code information

GE 25022900000 Peanut Butter Fudge Bar Cake 22.6 Oz

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 90334 with 9 other product entries in Public Health Trace.

Responsible company: Giant Eagle

Other recalls from Giant Eagle

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Pennsylvania	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of November 3, 2022.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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