UNFI General Corporate Recall: Eggs have been temperature abused.

🇺🇸 United States

1. August 2, 2020 - Recall initiated
2. September 2, 2020 - Reported by source
3. November 17, 2021 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1259-2020

Event ID

86160

Status

Terminated

Classification

Class II

Company

UNFI General Corporate

Product description

The following products received from the UNFI Distribution Center Champaign, IL on 7/12/2020: Ditch Farms Eggs brand: Grade A Large (20/18ct; UPC 2009194510035) and (30/12ct; UPC 1004127044750) and (30/6ct; UPC 1009194510032) ; Grade A Large Brown (30/12ct; UPC 2009194510060); Grade A Medium (20/1.5dz; UPC 2009194510060); and Vegetarian Brown Large (15/1dz, UPC 1071514111293). Dierbergs brand Grade A Xtra Large, 30/1dz; UPC 1002393300805 Egglands brand: Large Eggs (15/24ct, UPC 1071514160012); Organic Grade A Extra Large (15/12ct, UPC 71514162123); Organic Brown Large (15/12ct, UPC 71514160007); Large Brown (30/6ct, UPC 1071514160014); Cage Free Large Brown (15/12ct, UPC 1071514151564); Grade A Large (15/12ct, UPC 1071514150349) Everyday Essential brand Grade A Medium, 15/12ct, UPC 1004130302653)

Quantity

226 cases

Reason

Eggs have been temperature abused.

Recall initiation date

August 2, 2020

Report date

September 2, 2020

Classification date

Not published in this source record

Termination date

November 17, 2021

Distribution pattern

IN, IL, MO, WI

UPC, lot, and code information

UPC 2009194510035; Impacted Best By Dates: 8/6/2020 through 8/21/2020 ONLY UPC Codes received from UNFI DC Champaign, IL on Sunday 7/12/2020: Ditch Farms Eggs brand: UPC 2009194510035; UPC 1004127044750; UPC 1009194510032; UPC 2009194510060; UPC 1071514111293; UPC 2009194510025; UPC 2009194510026 Dierbergs brand: UPC 1002393300805 Egglands brand: UPC 1071514160012; UPC 71514162123; UPC 71514160007; UPC 1071514160014; UPC 1071514151564; UPC 1071514150349 Everyday Essential brand: UPC 1004130302653

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: UNFI General Corporate

Other recalls from UNFI General Corporate

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
Indiana	1
Illinois	1
Missouri	1
Wisconsin	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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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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