Albertsons Inc Recall: Discovered through the complaint process that the ingredient list for carrot cake slices did not include walnuts in the ingredient or allergen statement. Nuts are visible through packaging.

🇺🇸 United States

1. June 5, 2017 - Recall initiated
2. July 12, 2017 - Reported by source
3. July 12, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2412-2017

Event ID

77452

Status

Terminated

Classification

Class II

Company

Albertsons Inc

Product description

Carrot Cake Slice: Net Wt. 0 LB 7 OZ (198 g). Cake is assembled, iced, sliced and packaged at store level. Sliced wrapped individually in clear plastic clamshell and sold in bakery department. UPC Code: 0222132-000000 Sold under Albertsons Companies retail banners of Vons, Pavilions, Lucky and Albertsons.

Quantity

191,885 cake slices

Reason

Discovered through the complaint process that the ingredient list for carrot cake slices did not include walnuts in the ingredient or allergen statement. Nuts are visible through packaging.

Recall initiation date

June 5, 2017

Report date

July 12, 2017

Classification date

Not published in this source record

Termination date

July 12, 2017

Distribution pattern

Retail stores in CA

UPC, lot, and code information

All sell thru codes

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 Inc

Other recalls from Albertsons Inc

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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