Greenberg Fruit Co Recall: Routine environmental test samples were positive for Listeria monocytogenes on two processing machines.

🇺🇸 United States

1. July 15, 2016 - Recall initiated
2. October 12, 2016 - Reported by source
3. January 4, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2614-2016

Event ID

74749

Status

Terminated

Classification

Class I

Company

Greenberg Fruit Co

Product description

potato/sweet potato yam, Label states "Joe's Pride" and bears the address 9705 I Street, Omaha, NE 68127. Product is packaged in poly bags inside cardboard boxes. All products have a best by date of 7 days after the production date.

Quantity

4 cases (20 pounds each)

Reason

Routine environmental test samples were positive for Listeria monocytogenes on two processing machines.

Recall initiation date

July 15, 2016

Report date

October 12, 2016

Classification date

Not published in this source record

Termination date

January 4, 2018

Distribution pattern

Affected product was distributed to foodservice establishments in Omaha, Lincoln, and Bellevue, NE only.

UPC, lot, and code information

Lot number: 16076

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 74749 with 9 other product entries in Public Health Trace.

Responsible company: Greenberg Fruit Co

Other recalls from Greenberg Fruit Co

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
Nebraska	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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