RecallHawk
Class II Recall

UPC 22418000000 Platter Catering Loaf Cake Slice. This is Albertson's store-made item and so

Albertsons Companies LLC

Summary

The FDA issued a Class II for UPC 22418000000 Platter Catering Loaf Cake Slice. Th by Albertsons Companies LLC. Reason: Contains statement does not declare Walnut..

Details

Source

Food Recall

External ID

H-0959-2026

Action Date

2026-06-10

Status

Ongoing

Category

food

Product Description

UPC 22418000000 Platter Catering Loaf Cake Slice. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Lot/Code Info: Product was labeled with a Packed On date of May 05. 26 or before.

Quantity Affected: 92 units

Reason for Recall

Contains statement does not declare Walnut.

Distribution

Nationwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-05-06

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 166 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Albertsons Companies LLC has 174 FDA actions in our database, including 174 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Albertsons Companies LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Albertsons Companies LLC have FDA actions?

Albertsons Companies LLC has 174 FDA actions in our database, including 174 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0959-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions