Albertsons Inc Recall: Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.

🇺🇸 United States

1. October 20, 2017 - Recall initiated
2. November 15, 2017 - Reported by source
3. November 21, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0238-2018

Event ID

78352

Status

Terminated

Classification

Class I

Company

Albertsons Inc

Product description

Rectangular Vegetable Tray, 72 OZ UPC 24222100000 Sold in Albertson's and Safeway Stores packed in clear plastic trays and cups.

Quantity

231

Reason

Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.

Recall initiation date

October 20, 2017

Report date

November 15, 2017

Classification date

Not published in this source record

Termination date

November 21, 2017

Distribution pattern

Colorado, Nebraska, Northwestern New Mexico, South Dakota, Wyoming, California, Hawaii and Nevada.

UPC, lot, and code information

UPC 24222100000; Sell Thru Dates up to and including 10-24-17 (October 24, 2017)

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

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 78352 with 9 other product entries in Public Health Trace.

Responsible company: Albertsons Inc

Other recalls from Albertsons 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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