RecallHawk
Class II Recall

Signature Select Cookie Dough Ice Cream Vanilla Flavored ice cream with chocolate flavored chips and chunks of chocolat

Albertsons Companies LLC

Summary

The FDA issued a Class II for Signature Select Cookie Dough Ice Cream Vanilla Flavored ice cream with chocola by Albertsons Companies LLC. Reason: Signature Select Black Walnut Ice Cream was inadvertently packed in Cookie Dough container that does not declare nuts as allergen. Top lid correctly i.

Details

Source

Food Recall

External ID

F-0803-2022

Action Date

2022-03-09

Status

Terminated

Category

food

Product Description

Signature Select Cookie Dough Ice Cream Vanilla Flavored ice cream with chocolate flavored chips and chunks of chocolaty chip cookie dough. Artificial Flavor added. 1.5 qt. paper container. 6 retail units per case. UPC 2113008803 Some container were filled with Black Walnut Ice cream. Lid correctly identified product as Black Walnut Ice Cream.

Lot/Code Info: Best Before Mar 23 23 PLT 04 116 (1)

Quantity Affected: 258 retail units

Reason for Recall

Signature Select Black Walnut Ice Cream was inadvertently packed in Cookie Dough container that does not declare nuts as allergen. Top lid correctly identified Black Walnut flavor.

Distribution

Southern CA only

Type: Voluntary: Firm initiated

Recall Initiated: 2022-02-16

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 70 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 "F-0803-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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