Lower riskFood recall · FDA · Published June 10, 2026
Wells Dairy French Vanilla Pail Recall: Elevated Coliforms Risk
Wells Dairy recalls 1-gallon clear pails labeled 'BLUE RIBBON CLASSICS FRENCH VANILLA' due to elevated coliforms. Consumers should check product codes and contact Wells Dairy for details.
“Wells Dairy French Vanilla Pail Recall: Elevated Coliforms Risk.” GovInfoNow, updated August 7, 2026. https://govinfonow.com/recall/6189-wells-dairy-french-vanilla-pail-recall-elevated-coliforms-risk. Based on FDA recall #H-1151-2026.
The FDA announced on June 10, 2026, that Wells Enterprises, Inc. is recalling Plastic 1-gallon clear pails with blue labels reading "BLUE RIBBON CLASSICS FRENCH VANILLA" due to elevated coliforms. The recall affects one customer in Kenosha, WI.
How to tell if you have it
Brand: Wells Dairy
Product: BLUE RIBBON CLASSICS FRENCH VANILLA
Packaging: Plastic 1-gallon clear pail blue label
Lot code: 60003 JJJ 19115 18:00 6098
Best If Used By: 10/07/27
Pallet LPN: L7396434
Quantity: 195 cases
The hazard
The product may contain elevated coliforms, according to the FDA. The agency classified this as a Class II recall.
Context
GovInfoNow's records show Wells Enterprises, Inc. has issued three other recalls since May 2, 2014, including a foreign material hazard on April 25, 2025, and a Listeria risk on October 10, 2016. Other recent recalls of similar products include Dairy House Vanilla Dairy Powder (May 18, 2026), Twin Sisters Creamery Peppercorn Cheese (October 24, 2025), and Twin Sisters Creamery Farmhouse White Cheese (October 25, 2025).
How to tell if you have this one
Look for a clear plastic pail with a blue label that says 'BLUE RIBBON CLASSICS FRENCH VANILLA' and is manufactured by Wells Dairy. The product lot code starts with '60003' and has a best-by date of 10/07/27.
Brand
Wells Dairy
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the product label includes 'BLUE RIBBON CLASSICS FRENCH VANILLA' and the lot code starting with '60003'.
Where it went and when
Where it was distributed
Distributed in Wisconsin.
Listed by the agency
Not listed
FDA distribution: “One customer located in Kenosha, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Wisconsin.
Recall timeline
FDA terminated this recall 48 days after the firm started it.
1Firm started the recall
2Published in FDA’s Enforcement Report
3FDA classified it Class II
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-1151-2026 (June 10, 2026)
Plain-language summary written by qwen3:4b on August 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.