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