BIPC Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640008025, Item:
Summary
The FDA issued a Class II for BIPC Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le M by Wells Enterprises, Inc.. Reason: Foreign material (plastic) may be present in ice cream product.
Details
Source
Food Recall
External ID
F-0789-2025
Action Date
2025-05-21
Status
Terminated
Category
food
Product Description
BIPC Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640008025, Item: 934085
Lot/Code Info: Jet Code: LOT 50024 HH 19115 18:00 5105 USE BY OCT/14/26
Quantity Affected: 1858 3-gallon tubs
Reason for Recall
Foreign material (plastic) may be present in ice cream product
Distribution
103 distribution centers across the US
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-25
Company
Le Mars, IA
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 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Wells Enterprises, Inc. has 22 FDA actions in our database, including 22 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 (Wells Enterprises, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wells Enterprises, Inc. have FDA actions?
Wells Enterprises, Inc. has 22 FDA actions in our database, including 22 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0789-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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