Del Monte Fresh Produce Company Recall: The peanut butter in the snack items have the potential to be contaminated with Salmonella.

🇺🇸 United States

1. May 24, 2022 - Recall initiated
2. June 15, 2022 - Reported by source
3. August 9, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1266-2022

Event ID

90283

Status

Terminated

Classification

Class I

Company

Del Monte Fresh Produce Company

Product description

Del Monte Apple with Peanut Butter 5.5 oz UPC 717524102393 packaged in clear plastic non flexible container; Del Monte Apples & Peanut Butter dip 6 oz. UPC 717524720979 packaged in clear plastic non flexible container; Get Go Apples with Peanut Butter Dip Net Wt: 5 oz (142g) UPC 0030034937706 packaged in clear plastic non flexible container

Quantity

2448 units

Reason

The peanut butter in the snack items have the potential to be contaminated with Salmonella.

Recall initiation date

May 24, 2022

Report date

June 15, 2022

Classification date

Not published in this source record

Termination date

August 9, 2022

Distribution pattern

FL, IN, PA, TX and OK

UPC, lot, and code information

UPC 717524102393; Best If Used By 5/24/2022- 5/30/2022

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 90283 with 3 other product entries in Public Health Trace.

Responsible company: Del Monte Fresh Produce Company

Other recalls from Del Monte Fresh Produce Company

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
Florida	1
Indiana	1
Pennsylvania	1
Texas	1
Oklahoma	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.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

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?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

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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