Albertsons Companies LLC Recall: A temperature data logger which is intentionally placed into one container of soup to monitor cooling has been misplaced and believed to be in a retail package.

🇺🇸 United States

1. February 25, 2019 - Recall initiated
2. March 20, 2019 - Reported by source
3. March 12, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1159-2019

Event ID

82262

Status

Terminated

Classification

Class II

Company

Albertsons Companies LLC

Product description

Signature Caf¿ Tomato Basil Bisque Soup: polypropylene cups with linear low density polyethylene caps, and with plastic film seal. NET WT: 24 oz. (1 lb.. 8 oz.) 680 g Perishable, Keep Refrigerated. UPC 0002113015645 Distributed by: Lucerne Foods, Inc., P. P. Box 99, Pleasanton, CA 94566-0009

Quantity

500 cases (8 cups per case)

Reason

A temperature data logger which is intentionally placed into one container of soup to monitor cooling has been misplaced and believed to be in a retail package.

Recall initiation date

February 25, 2019

Report date

March 20, 2019

Classification date

Not published in this source record

Termination date

March 12, 2019

Distribution pattern

Shipped to distribution center in Fullerton, CA and the on to retail stores in CA,

UPC, lot, and code information

UPC 0002113015645; Sell By April 24, 2019

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: Albertsons Companies LLC

Other recalls from Albertsons Companies LLC

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
California	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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