Cedar Crest WI Campfire S'Mores Ice Cream, Net Wt. 1.5 Quarts (1.41 L). UPC 20652-00768. Graham Flavored Ice Cream wi
Summary
The FDA issued a Class II for Cedar Crest WI Campfire S'Mores Ice Cream, Net Wt. 1.5 Quarts (1.41 L). UPC 206 by Cedar Crest Specialties, Inc.. Reason: Foreign material - plastic.
Details
Source
Food Recall
External ID
F-1296-2022
Action Date
2022-06-22
Status
Terminated
Category
food
Product Description
Cedar Crest WI Campfire S'Mores Ice Cream, Net Wt. 1.5 Quarts (1.41 L). UPC 20652-00768. Graham Flavored Ice Cream with Crushed Peanut Butter cups and Marshmallow Swirl. Cedar Crest Specialties, Inc. Cedarburg, WI 53012
Lot/Code Info: Lot 3001 (on bottom of container)
Quantity Affected: 10,036 units
Reason for Recall
Foreign material - plastic
Distribution
IL, MI, MN, TX, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-17
Company
Manitowoc, WI
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 175 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Cedar Crest Specialties, Inc. has 2 FDA actions in our database, including 2 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 (Cedar Crest Specialties, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Cedar Crest Specialties, Inc. have FDA actions?
Cedar Crest Specialties, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1296-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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