Weis Quality Premium Ice Cream Sea Salt Caramel Ripple 1.5 Quart (1.42 L) UPC 041497-01288
Summary
The FDA issued a Class II for Weis Quality Premium Ice Cream Sea Salt Caramel Ripple 1.5 Quart (1.42 L) UPC 04 by Weis Markets, Inc., Ice Cream Division. Reason: Undeclared soy and coconut.
Details
Source
Food Recall
External ID
F-0190-2023
Action Date
2022-12-14
Status
Terminated
Category
food
Product Description
Weis Quality Premium Ice Cream Sea Salt Caramel Ripple 1.5 Quart (1.42 L) UPC 041497-01288
Lot/Code Info: Sell by date: 11/08/23
Quantity Affected: 108 containers
Reason for Recall
Undeclared soy and coconut
Distribution
Distributed to retail stores in Pennsylvania, Maryland, Virginia, New Jersey, New York, Delaware and West Virginia.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-11-23
Company
Sunbury, PA
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 16 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Weis Markets, Inc., Ice Cream Division has 6 FDA actions in our database, including 6 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 (Weis Markets, Inc., Ice Cream Division) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Weis Markets, Inc., Ice Cream Division have FDA actions?
Weis Markets, Inc., Ice Cream Division has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0190-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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