Jac Vandenberg Inc. Recall: Product may be contaminated with Listeria monocytogenes.

🇺🇸 United States

1. January 22, 2019 - Recall initiated
2. February 6, 2019 - Reported by source
3. July 9, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1052-2019

Event ID

81965

Status

Terminated

Classification

Class I

Company

Jac Vandenberg Inc.

Product description

Nectarines sold as a bulk retail item, with PLU 3035 (white flesh nectarine) and 4378 (yellow flesh nectarine), and country of origin of Chile. The nectarines sold at Aldi are packaged in a two pound bag with EAN 7804650090298. The nectarines sold at Costco are packaged in a 4-pound plastic clamshell with the brand Rio Duero, EAN# 7804650090212.

Quantity

3299 cartons (total for all products)

Reason

Product may be contaminated with Listeria monocytogenes.

Recall initiation date

January 22, 2019

Report date

February 6, 2019

Classification date

Not published in this source record

Termination date

July 9, 2019

Distribution pattern

Alabama, California, Georgia, Illinois, Kentucky, Maine, Massachusetts, Michigan, Mississippi, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Tennessee, West Virginia and Virginia

UPC, lot, and code information

N/A

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

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 81965 with 2 other product entries in Public Health Trace.

Responsible company: Jac Vandenberg Inc.

Other recalls from Jac Vandenberg Inc.

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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