Class IITerminatedVoluntary: Firm initiated
Wells Enterprises, Inc.: food recall H-1151-2026
Wells Enterprises, Inc. of Le Mars, IA recalled Plastic 1-gallon clear pail blue label which reads in part as "BLUE RIBBON CLASSICS FRENCH VANILLA, MFD. BY WELLS… Reason: Elevated coliforms. The FDA listed it as Class II in its Enforcement Report dated Jul 8, 2026; distribution: Wisconsin.
Record status as published: Terminated (terminated Jul 28, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 195 cases
- Reason for recall
- Elevated coliforms
- Codes, lots and dates on the package
- Pallet LPN: L7396434 Product lot code: 60003 JJJ 19115 18:00 6098 Best If Used By 10/07/27
- Distribution pattern
- One customer located in Kenosha, WI
- Recalling firm
- Wells Enterprises, Inc., Le Mars, IA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jun 10, 2026 |
| Classified by the FDA | Jul 13, 2026 |
| Published in the Enforcement Report | Jul 8, 2026 |
| Terminated | Jul 28, 2026 |
Other recalls by Wells Enterprises, Inc.
- F-0800-2025 · May 21, 2025 · Class II — Foreign material (plastic) may be present in ice cream product
- F-0799-2025 · May 21, 2025 · Class II — Foreign material (plastic) may be present in ice cream product
- F-0798-2025 · May 21, 2025 · Class II — Foreign material (plastic) may be present in ice cream product
- F-0797-2025 · May 21, 2025 · Class II — Foreign material (plastic) may be present in ice cream product
- F-0796-2025 · May 21, 2025 · Class II — Foreign material (plastic) may be present in ice cream product
- F-0795-2025 · May 21, 2025 · Class II — Foreign material (plastic) may be present in ice cream product
- F-0794-2025 · May 21, 2025 · Class II — Foreign material (plastic) may be present in ice cream product
- F-0793-2025 · May 21, 2025 · Class II — Foreign material (plastic) may be present in ice cream product
- F-0792-2025 · May 21, 2025 · Class II — Foreign material (plastic) may be present in ice cream product
- F-0791-2025 · May 21, 2025 · Class II — Foreign material (plastic) may be present in ice cream product
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-1151-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.