Plastic 1-gallon clear pail blue label which reads in part as "BLUE RIBBON CLASSICS FRENCH VANILLA, MFD. BY WELLS ENTERP
Summary
The FDA issued a Class II for Plastic 1-gallon clear pail blue label which reads in part as "BLUE RIBBON CLASS by Wells Enterprises, Inc.. Reason: Elevated coliforms.
Details
Source
Food Recall
External ID
H-1151-2026
Action Date
2026-07-08
Status
Ongoing
Category
food
Product Description
Plastic 1-gallon clear pail blue label which reads in part as "BLUE RIBBON CLASSICS FRENCH VANILLA, MFD. BY WELLS ENTERPRISES, INC. D/B/A WELLS DAIRY, INC., P.O. BOX 1310 LE MARS, IA 51031
Lot/Code Info: Pallet LPN: L7396434 Product lot code: 60003 JJJ 19115 18:00 6098 Best If Used By 10/07/27
Quantity Affected: 195 cases
Reason for Recall
Elevated coliforms
Distribution
One customer located in Kenosha, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2026-06-10
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 55 food recalls issued in the same week, part of 81 food-related FDA actions this month.
Wells Enterprises, Inc. has 23 FDA actions in our database, including 23 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 23 FDA actions in our database, including 23 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1151-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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